Assessment and modification of a human subject&#39;s circadian cycle

ABSTRACT

A method for modifying the human endogenous circadian pacemaker is disclosed. The method comprises the steps of determining the characteristics of a desired endogenous circadian cycle for a subject; selecting an appropriate time with respect to the presumed phase of physiological markers of the present endogenous circadian cycle for the subject during which to apply a light stimulus to effect a desired modification of the present endogenous circadian cycle of the subject; and applying said light stimulus at said selected appropriate time to achieve the desired endogenous circadian cycle for the subject. The method finds special utility in treating &#34;jet lag&#34; sufferers, shift workers, advanced circadian phase experienced by many elderly subjects, and those afflicted with delayed sleep phase insomnia.

studies. Each point shows the mean (±SEM) for each variable at a given time of day during initial (open symbols) and final (closed symbols) constant routines. Vertical dashed line indicates the starting time of the night shift (midnight). Conditions during the control and treatment studies as described in FIG. 18B.

FIG. 19 is a world map indicating the adjustment to transmeridian travel which would be simulated by the specific experiment illustrated in FIG. 18.

FIG. 20 shows a prototypical schedule for achieving a small phase delay (about 3 hours).

FIG. 21 shows how bright light can reset the circadian oscillator independent of the timing of sleep/darkness: the use of evening bright light to treat advanced circadian phase.

FIG. 22 shows phase displacement of cortisol rhythm following exposure to light in a patient with advanced circadian phase.

FIG. 23 is a raster plot of laboratory simulation of world travel, including phase advances and phase delays of varying magnitude.

FIG. 24 is a graphical representation of itinerary simulated in FIG. 23.

FIG. 25 shows a prototypical schedule for achieving a small phase advance (about 3 hours).

FIG. 26 shows fitted temperature data showing an approximately 3-hour phase advance in the circadian pace maker of a patient with Delayed Sleep Phase Syndrome.

FIG. 27 is a raster plot of protocol used in the assessment and treatment of the patient described in FIG. 26.

FIG. 28 shows pre- and post-intervention assessments of circadian phase of a jet traveler flying from the orient to Boston.

FIG. 29 is a graphical representation of the traveler whose circadian phase was assessed in FIG. 28.

FIG. 30 is a raster plot of travel log, assessment, and treatment of the traveler of FIG. 28.

FIG. 31 is an actual timing diagram of the core body temperature of a subject whose endogenous circadian pacemaker has been driven to zero amplitude.

FIG. 32 shows how circadian amplitude is increased with light

FIGS. 33A, 33B and 33C show the separate, and the summed, Brightness function B(t) and the Activity function A(t), along with the resultant stimulus vector using a Fourier fundamental.

FIG. 34 shows a phase shift diagram, illustrating the two types of resetting curves which show resultant phase shift as a function of the phase of the stimulus vector.

FIG. 35 shows amplitude response as a function of stimulus vector circadian phase for various numbers of 24-hour cycles.

FIG. 36 shows the model's concordance with actual experimental data.

FIG. 37 is a phase-plane diagram illustrating the use of bright light pulses to reduce the amplitude of the endogenous circadian pacemaker to near the mathematical "singular point".

FIG. 38 is a timing diagram corresponding to the phase-plane diagram of FIG. 37.

FIG. 38A is a timing diagram which illustrates the reduction in effective amplitude of the endogenous circadian pacemaker to near zero in less than 1.5 days, representing an acceleration of the effects shown in FIG. 38.

FIG. 39 is a sketch of a representative lighting appliance.

FIGS. 40A and 40B are a sketch of a representative light goggle with peripheral hardware and software.

FIG. 41 shows, in vector form, changes produced by light lo in the variables x and x_(c) for a variety of reference (x,x_(c)) points (i.e., x and x_(c) corresponding to the midpoint of bright episodes).

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

A first method is directed to the accurate assessment of the phase and amplitude resetting capacity of the endogenous circadian pacemaker for a particular subject within a relatively short time frame. A second method is directed to the actual modification of the phase and/or amplitude of that pacemaker using scheduled periods of bright light, advantageously enhanced with manipulation of dark (rest) periods, based on either normative phase assessments or on a phase assessment of that individual subject. Phase and amplitude modification may be achieved based on either empirically derived normative data or based on a mathematical model, relating to the existing state of the deep circadian pacemaker. Finally, devices which facilitate the practice of the assessment and modification methods are described.

1. Foundations for the Inventive Techniques of Assessing Circadian Phase and Amplitude Resetting Capacity

As stated above in the Background of the Invention, there have been a variety of lengthy techniques used to try to assess the phase resetting capacity of the circadian timing system, none of which was ideally suitable for use in humans. The most commonly used technique used in animal studies, delivery of a stimulus during a synchronized free-run, is an inadequate means of testing the response capacity of the human circadian system to a signal. This is because after disturbance of the sleep-wake cycle the body temperature cycle would no longer oscillate at the compromise period it displays during a synchronized free run (T_(S)) which is usually longer than its intrinsic period (T_(X)), but would instead oscillate for 1-2 cycles at its intrinsic period. This would make most signals appear to cause a modest phase advance, as occurs in response to one night of sleep deprivation (see C. A. Czeisler et al., "Sleep Deprivation in Constant Light Phase Advance Shifts and Shortens the Free-Running Period of the Human Circadian Timing System," Sleep Research, Volume 14, p. 252. See also Honma, K., Honma, S., Wada, T., "Phase Dependent Responses of Human Circadian Rhythms to a Bright Pulse: Experiments in a Temporal Isolation Unit", J. Physol. Soc. Jap., Vol. 48, p. 416 (1986).). In addition, the free-running rest-activity cycle is not an accurate marker of the endogenous circadian phase in human subjects.

Thus, we designed a technique to combine a method to rapidly assess the phase and amplitude of the endogenous circadian pacemaker before and after delivery of a stimulus protocol. With the stimulus protocol itself.

Presently, the most widely recognized method to assess the phase and amplitude of the endogenous circadian oscillator is to track the body temperature cycle during long-term studies where behavioral activity is desynchronized from the output of the endogenous oscillator, thereby distributing masking effects of activity on the temperature cycle across a variety of temperature phases. Typically, this assessment method is carried out prior to, and following a particular intervention in order to assess the effect of that intervention on the circadian oscillator. However, since masking effects are not in any way eliminated, each of the assessments require the collection of 4-6 weeks of continuously recorded data in a time-isolated facility. Following spectral analysis of the data, an endogenous circadian period is determined. Using this period, an average waveform is educed. Endogenous circadian phase and amplitude are determined from this educed waveform. For statistical reasons, this estimate is most accurate only for days in the middle of the study, and achieves its greatest inaccuracies at the beginning and end of the study. Also, because this method is dependent upon an accurate period assessment, a misestimation of period, when iterated over the length of the study, can result a several hour misestimation of phase at the beginning or end of the study.

Because this method is inaccurate in initial and final phase estimation, it is unsuited to be used as the "before" and "after" assessment components of an experimental protocol designed to test the effect of a particular invention. Additionally, their length is prohibitively long for practical use.

In the following section we describe a technique which is able to characterize the output of the endogenous circadian pacemaker in a brief time. This has utility both in identifying circadian dysfunction and in developing a body of normative data on circadian function. Most importantly, in a preferred embodiment consisting of two such assessments, one immediately prior to and one following an intervention, this method provides a means of assessing the ability of a particular intervention to modify circadian phase and amplitude. In this regard, this new method and its preferred embodiments have provided a means both for development and validation of the empirical methods upon which our techniques of modifying circadian phase and amplitude are based.

The preferred embodiment of the method of accurately assessing the phase and amplitude of the deep circadian pacemaker is premised on the elimination of confounding factors which would otherwise mask the measurement of the phase. The confounding factors introduced by food ingestion, changes in posture, changes in physical activity, sleep onset and waking are eliminated according to the preferred embodiment of the present invention. Generally, the effects of these factors on the phase measurement are minimized by eliminating them, or at least distributing them evenly over the course of the phase measurement process.

2. Method for assessment of circadian phase and amplitude resetting capacity

The preferred embodiment of the method for assessment of circadian phase and amplitude resetting capacity is based upon a comparison between a pre-intervention phase and amplitude assessment and a post-intervention phase and amplitude assessment. The pre-intervention assessment characterizes the baseline status of the circadian timing system. It also provides a phase and amplitude reference useful in the subsequent determination of the appropriate time(s) to schedule the intervention stimulus. The post-intervention assessment provides a final characterization of the circadian system so that an objective assessment of the efficacy of the intervention can be made.

FIG. 1 shows an example of the preferred embodiment of the method for assessment of circadian phase and amplitude resetting capacity. In this particular study, a human subject was studied for seven days in an environment free of time cues. The schedule of this embodiment of the assessment technique is presented in double raster format as described below (e.g., in the discussion relating to FIGS. 8 and 18). The first thirty to forty hours of the study (represented by an open bar) constitute the pre-intervention phase and amplitude assessment. Days 2-5 comprise the particular intervention stimulus under study. The final 40 hours (represented by an open bar) depicts the post-intervention assessment of phase and amplitude. It is necessary to detect and account for the free-running phase delay which occurs in the Constant Routines. Thus, a correction factor related to the free-running deep circadian pacemaker period T_(X) must be considered when formulating conclusions regarding the effect of the intervening experiment.

In this example, the intervention stimulus chosen was a particular light schedule consisting of bright indoor light (large boxes) and episodes of darkness/sleep (solid bars). However, the intervention stimulus chosen may be of any nature (i.e., a pharmaceutical agent or other therapy). In this example, the duration of the intervention stimulus was approximately 3.5 days. However, the intervention stimulus may take on any duration, shorter or longer, depending upon the nature of the particular intervention.

The pre- and post-intervention assessments of phase and amplitude are advantageously embodied in a technique called the "Constant Routine". The Constant Routine involves keeping the subject at absolute bedrest in a semi-recumbent posture (i.e., lying in bed with the head of the bed (from the waist up) advantageously elevated at an approximately 45 degree angle, and the knees elevated and supported advantageously to provide approximately 90 degrees between the back of the calf and the back of the thigh). This ensures that changes in the physical posture do not influence the phase or amplitude assessment. The subject refrains from any physical activity, since physical activity might also influence or distort the phase measurement. In practice, arm and head movement, and general shifting of body weight in the semi-recumbent posture, are allowable. However, the torso should not be elevated from the bed, even for brief periods.

The subject is kept awake in ordinary room light throughout the duration of the assessment so that sleep onset or offset and changes in ambient light levels also do not affect the phase measurement. Finally, to minimize the effects of food intake which would result from a normal schedule of large meals, the subject ingests measured small amounts of food at closely spaced intervals, such as hourly. The food is advantageously chosen to emulate the daily nutritional intake of the individual during a normal day, with the subject on an isocaloric diet, with caloric intake calculated using the Wilmore nomogram, with balanced electrolyte intake of 150 millequivalents of sodium and 100 millequivalents of potassium per 24 hours. This effectively continuous feeding ensures that any effect of food ingestion on the phase measurement is evenly distributed throughout the duration of the phase measurement technique.

Assessment of physiologic parameters is advantageously achieved by continuous measurements of core body temperature via a thermistor inserted 10 cm. into the rectum, a skin temperature thermistor worn on the inner--aspect of the non-dominant wrist; polysomnographic recording from surface electroencephalographic (central , frontal and occipital placements), electromyographic and electrooculographic electrode placements; an intravenous placement unit in a forearm vein for multiple frequent sampling of blood (3 samples per hour) without repeated venipuncture; cognitive and behavorial alertness and performance measures; and other techniques well known in the art. The overall Constant Routine protocol is illustrated in FIGS. 2A and 2B, and is further explained in the discussion directed to FIGS. 3, 4, and 7.

The measurements are then advantageously plotted as a function of time for statistical analysis. Advantageously, statistical analysis using harmonic regression techniques may be used to calculate the amplitude of the endogenous temperature rhythm, and to pinpoint the time of the endogenous temperature cycle minimum, which serves as a marker of circadian phase. For example, see Brown, Sleep Research, Vol. 14, p. 90 (1985).

In particular cases, the endogenous circadian phase can be assessed, for example, by using non-linear least-squares to fit a 2-harmonic regression model to the core body temperature data recorded during the Constant Routine (excluding a period of time at the beginning of the Constant Routine, such as 5 hours). The 2-harmonic regression model can be fit to the data and an average of the minima from the single harmonic and composite waveforms of the model can be used as the reference marker of endogenous circadian phase (ECP_(min)) for these studies. These methods are described, e.g., by E. N. Brown, M.D. thesis, Harvard University (1987). Of course, variations on the determination of the ECP minimum lie within the contemplation of the invention. Indeed, desired phase shifting and/or amplitude modification may be achieved without a formal "assessment" procedure. However, the above described mathematical determination method removes subjective estimation, and, consistently used, allows meaningful comparisons to be made across different studies.

Other researchers have considered many of the confounding factors which are eliminated by the Constant Routine. However, what was missing in many such experiments was the correct bracketing of the initial estimate of the deep circadian pace-maker minimum. In the absence of a reasonable estimate of the timing of this minimum, other experimenters did not choose a duration long enough to ensure that each phase assessment exposed at least one unobscured minimum of the endogenous circadian temperature cycle, as is advantageously ensured by a 40-hour Constant Routine according to an embodiment of the present invention.

It is advantageous that the subject remain in this Constant Routine for at least one and one-half full periods of his or her endogenous circadian pacemaker. Generally, this period is approximately 25 hours. In one embodiment of the present invention, the full duration of the Constant Routine is 40 hours. A 40-hour Constant Routine allows several hours at the beginning of the Constant Routine to dissipate any transient effects of the subject's sleep episode or other activities immediately before the Constant Routine. It has been found that approximately 4-5 hours at the beginning of the Constant Routine are necessary to dissipate the effect of those activities. Using a full 40-hour Constant Routine ensures that at least one unobscured endogenous circadian pacemaker minimum is measured without any effect being imposed by the transient response to the subject's activity immediately prior to the Constant Routine.

In another embodiment of the assessment method according to the present invention, a Constant Routine of duration much shorter than 40 hours may be successfully practiced. The use of this shorter assessment method is premised on knowledge of the approximate time of the minimum of the endogenous circadian pacemaker minimum. It is desirable that 6-8 hours of core body temperature measurements both before and after the deep circadian pacemaker minimum be recorded, in order to accurately determine the minimum using, for example, mathematical techniques described by Brown, cited above. Therefore, it is conceivable that a Constant Routine of a duration as short as 16 hours can be applied. (2×6 hours surrounding the minimum+4 hours to dissipate the transient effects=16 hours.)

Since, especially in longer-duration Constant Routines, the period of imposed wakefulness may prove burdensome to many subjects, it is preferred that Constant Routines are timewise flanked by periods of darkness/sleep. These periods of darkness/sleep must be considered when assessing the effects of the bright light/darkness regimen on a particular subject, since the periods of darkness themselves have a strong effect on the phase and amplitude modification being investigated. In most experimental scenarios, a Constant Routine is entered both before and after the regimen of bright light pulses and darkness periods. The periods of darkness which flank both Constant Routines are an integral part of the stimulus regimen, and are advantageously scheduled to enhance the phase-shifting characteristics of the regimen.

FIG. 3 shows the daily patterns of several physiologic and cognitive functions in a single young male subject on a normal day and during a phase and amplitude assessment procedure. A fitted dual harmonic regression model of the body temperature data during the Constant Routine is shown in Panel A, superimposed on the actual body temperature data. Time is plotted along the horizontal axis; dark bars and stippled areas indicate episodes of sleep the cross hatched bar represents the time of the Constant Routine. In comparing data collected during the Constant Routine days with that of the previous entrained day, one can see the persistent oscillation of the endogenous component of the observed rhythms, which is prominent in the case of core body temperature, subjective alertness, serum cortisol secretory pattern, and urine volume; such oscillations are no longer detectable in the activity level, and growth hormone secretion ceases under these constant conditions. By fitting the endogenous component of the temperature rhythm with a harmonic regression curve (as has been done in the upper panel of this figure), an estimate of the amplitude and fitted phase of the temperature minimum (marked by the encircled cross) of the endogenous circadian pacemaker can be made.

FIG. 4 shows normative data collected from 29 normal young male subjects. The protocol is indicated in the top legend, with symbols as in FIG. 2A. B, L, D, S mean breakfast, lunch, dinner, snack, respectively, before the Constant Routine was entered. Panel A--core body temperature (N=29); Panel B--subjective alertness (N=27); Panel C--serum cortisol (N=23); Panel D--urine volume (N=28); Panel E--Human Growth Hormone; and Panel F--wrist activity (N=18). The data are normalized with respect to the subjects' habitual reference waketime (RW), and are plotted in a manner similar to that of FIG. 3. Additionally, data from the entrained day are superimposed (dotted lines) during the Constant Routine period to facilitate comparison between the entrained (masked rhythm) and the unmasked Constant Routine waveforms. Note how the Constant Routine temperature data from the individual subject in FIG. 3 closely matches that of the normative population, allowing accurate comparison of data recorded on a single individual with that of the normative population.

FIG. 5 shows a histogram of the estimated phase of the endogenous circadian temperature minimum, based on data collected from 29 normal male subjects with no history of circadian disruption (i.e., shift-work, transmeridian travel, or disturbed sleep) after their second night living in the laboratory. As can be seen, most subjects reached their endogenous temperature minimum approximately 1.5±1.0 hours before their habitual waketime.

Normative data for subjects of various ages is shown similarly in FIGS. 6A and 6B. In FIG. 6B, one can see that the amplitude of the temperature rhythm measured during the Constant Routine is lower in the elderly population (65-85 years of age). FIG. 6B shows that the phase of the endogenous circadian temperature rhythm occurs earlier in the elderly than in the young normal males.

FIG. 7 demonstrates the unmasking effect of the Constant Routine according to a preferred embodiment of the method according to the present invention. FIG. 7 illustrates the core body temperature of four subjects as a function of time. The top panel presents the core body temperature of a normal young subject; the second panel, that of an elderly subject with advanced circadian phase; the third, that of a young adult with Delayed Sleep Phase Syndrome; and the bottom, that of an elderly subject with reduced amplitude.

For all four subjects, the Constant Routine commences at time 0800 on the first full day, as illustrated at 200. The Constant Routine continues for 40 hours until the end of the second full day. The duration of the Constant Routine is indicated on the time axes to the right of 200. Before the Constant Routine was initiated (to the left of 200), the core body temperature of each subject was monitored, starting at noon on the day before the Constant Routine.

All four panels illustrated in FIG. 7 have plotted normative data 204, 212, and 220 for comparison to various individual core body temperature plots 202, 210, and 218. The normative data plots 204, 212, and 220 are identical.

As can be seen in the pre-Constant Routine period to the left of 200, all four subjects' core body temperature followed the normative data with a high degree of correlation, which was directly linked to the activity of the subjects. Before the onset of the Constant Routine, then, it would have been impossible to accurately determine the endogenous circadian pacemaker amplitude or phase because of the activity-induced core body temperature responses.

Before engaging in the Constant Routine, all four subjects appeared to be normal, based on observation of core body temperature. In fact, however, only the subject illustrated in the top panel was normal.

The top panel of FIG. 7 shows a 20-year-old male whose measured core body temperature coincided with the trough of the normative data at 206. His endogenous circadian pacemaker minimum, as indicated by the core body temperature minimum, was timed optimally for a regular waking time (RW) of 8:00 a.m. This subject reported no abnormalities or difficulties in his sleeping habits.

The second panel shows the core body temperature of a 66-year old woman suffering from extreme phase-advancement, characteristic of many elderly subjects. Her measured deep circadian pacemaker trough 214 was in fact 4.5 standard deviations earlier than the trough 216 of the young subjects contributing to the normative data plot 212. In contrast, the core body temperature trough of the normal young subject in the upper panel is synchronized to the measured deep circadian pacemaker minimum at 206.

The third panel illustrates the core body temperature from a young patient suffering from Delayed Sleep Phase Insomnia. This subject had reported great difficulty in awakening in the morning and remaining alert. This difficulty is explained by the fact that his internal physiology did not even begin to "awaken" until about noon. The third panel of FIG. 7 illustrates his core body temperature trough at 224 as being approximately 4 hours past his regular wake time, 8:00 a.m. This trough 224 is also significantly delayed from the normative data trough at 222.

The bottom panel illustrates the reduced amplitude characteristic of many elderly subjects. The significance of this reduced amplitude is discussed below.

The core body temperature troughs indicated at 206, 214, and 224 were unmasked by the Constant Routine. These troughs indicate the tendency of the deep circadian pacemaker to establish its own period and phase which are demonstrable in the absence of activity-induced body temperature changes. A value of the Constant Routine in eliminating physiologic responses to environmental and behavioral stimuli lies in diagnosing such phase advance or phase delay disorders. Once diagnosed, these disorders may be treated according to a method of phase-shifting according to the present invention, described below.

The preferred embodiment of the assessment method is far less time-consuming than the assessment methods described previously which require temporal isolation for a time period on the order of 30 days. The method of assessment according to the present invention thus allows clinical observation in cases where extremely accurate individual phase and amplitude measurements must be made. The present method also allows the gathering of extremely accurate normative data which can later be used in the phase adjustment of large classes of people who are similarly situated with respective classes of subjects whose circadian cycles' characteristic phase and amplitude have already been assessed using the Constant Routine.

3. Empirical Foundations for the Inventive Techniques to Modify Circadian Phase and Amplitude

Aschoff and Wever in Germany and Siffre in France discovered that numerous daily rhythms in man also persist in the absence of environmental and social time cues. However, under these conditions of temporal isolation, the "free-running" period of these rhythms no longer remained exactly 24 hours (FIG. 8).

Referring to FIG. 8, a raster diagram of the sleep episodes of a subject in temporal isolation is illustrated. The horizontal time axis is referenced to the subject's habitual bed time (hour 0), as recorded in a home sleep-wake diary during the prior week. Successive days are plotted beneath each other. Scheduled sleep/dark intervals (outlined by a black box) were from hours 0 to 7 on days 1-20. Thin horizontal lines indicate time span awake in bed; time asleep (as determined polysomnographic recording) is indicated by heavy black horizontal bars. Thin vertical lines indicate self-selected bed times and times of rising.

Generally, raster diagrams have a series of time axes, each of which traverses continuously from left to right. Each horizontal time axis is labelled with a "Day n" number which indicates the 24-hour period which is presented in the left-most 24 hours of that time axis. Information about days immediately succeeding "Day n" may be illustrated to the right of the leftmost 24-hour period in the "Day n" axis. (In some raster displays--unlike FIG. 8--information from the Day n axis may actually be repeated, but left-shifted by 24 hours, on the Day n+1 axis.) Raster diagrams thus provide a convenient means by which temporal activities and conditions may be analyzed both in a serial fashion (horizontally), and in a parallel fashion (vertically) for comparison.

Referring again to the particular raster diagram in FIG. 8, during Days 1-20 of the experiment, the subject was forced to keep a regular schedule synchronized to the 24-hour geophysical day, as indicated at 102. The subject's circadian cycle was thus "entrained" to a 24-hour period.

After the 21st day, the subject was allowed to choose when to sleep, awaken, eat, etc., naturally, his schedule being governed only by his internal circadian pacemakers. Consistent with previous experimental results in humans and diurnal animals, from Days 21-53 the subject's activity-rest cycle and core body temperature cycle both assumed their "free running" (but mutually synchronized) periods of greater than the previously entrained period of 24 hours. The assumption of a period longer than 24 hours is indicated in FIG. 8 as a gradual but steady phase delay in both the bed rest episodes. The free-running period was determined by linear regression through midsleep times to be 25.3 hours.

The first 20 days of the experiment depicted in FIG. 8 are indicative of the "normal" days experienced by the majority of humans. Their internal circadian cycle periods of greater than 24 hours are overridden, or reset, by some zeitgeber. It was thought that only zeitgebers such as social contact or imposed activity could reset the human circadian cycle to the 24-hour geophysical day. As will be seen below, humans are in fact no exception to the rule in the animal kingdom that light, in and of itself, is a strong zeitgeber.

Ordinary sunlight, then, apparently resets at least the deep circadian pacemaker on a daily basis to a 24-hour cycle. This resetting allows humans to function in activities which are necessarily tied to the 24-hour geophysical day. If the circadian cycles of humans were not reset on a daily basis, the free-running cycle of greater than 24 hours would cause disruption of individuals' performance not only with respect to the geophysical day, but also with respect to other individuals' free-running but mutually desynchronized circadian cycles.

Concomitant with the discovery of non-twenty-four hour free-running circadian rhythms in humans came the assumption that humans, like all other eukaryotic organisms studied, must have a mechanism of entrainment receptive to exogenous time cues (Zeitgeber) which would allow synchronization to the twenty-four hour geophysical day. The effect of an entraining agent, such as a light pulse in otherwise constant darkness, on circadian rhythms has been studied extensively in a variety of species, ranging from single-celled eukaryotes to primates. It is therefore possible to describe the effect of a single light pulse in otherwise constant darkness by means of a phase response curve which indicates that under such conditions the phase of administration of the light pulse alone determines the magnitude and direction of the phase shift elicited.

Although it was generally accepted that the light-dark cycle was the most potent resetting stimulus in almost all eukaryotic organisms, much debate arose as to the nature of the principal resetting stimulus in humans. Based on a series of temporal isolation studies, Aschoff and Wever concluded that a 24-hour light-dark cycle was too weak an entraining stimulus to mediate the approximately one hour phase resetting necessary for synchronization to the 24-hour geophysical day. A critical review of the experimental protocol revealed that the subjects of Aschoff and Wever were in fact self-selecting much of the lighting in the experimental suite. It is therefore not surprising that a free-running pattern emerged. Subsequent studies under more rigorous control have revealed that a light-dark cycle alone is capable of entraining the human circadian timing system to a twenty-four hour day. (See C. A. Czeisler et al., "Entrainment of Human Circadian Rhythms by Light-Dark Cycles: A Reassessment," Photochemistry and Photobiology, Vol. 34, pp. 239-249 (1981)). It was not known, however, whether this entrainment was the result of a direct action of light on the central hypothalamic pacemaker or whether it was simply due to the light-dark cycle's indirect influence on the behavioral choice of bedtime and wake-time.

Unfortunately, physiologists had been unable to demonstrate an unequivocal direct effect of bright light on human circadian rhythms, primarily because of a lack of experimental techniques to directly assess circadian phase in real time. The development of the aforementioned means of assessment of phase and amplitude resetting capacity has now yielded a better understanding of the interaction between the human biological clock and periodic environmental stimuli than had been afforded by the animal studies carried out under the rather simplistic and clinically irrelevant condition of total darkness.

As will be described below, applications of bright light may be artificially imposed to achieve effects other than mere resetting to the geophysical day. It will be seen that bright light can be used to achieve dramatically rapid shifting of circadian phase. Very significantly, the application of bright light can have a direct influence on the deep circadian pacemaker, independent of the timing of activity-related factors.

Based on application of the above assessment technique, the present invention is partially based on the determined circadian effects of numerous different illumination schedules, all consisting of components of bright light, ordinary indoor light, and absolute darkness. The invention is partially based on newly discovered general properties of the human circadian pacemaker's response to light-dark cycles. These can be summarized as follows:

A. Bright light is required to shift rapidly the phase of the circadian pacemaker. That is to say that shifting the timing of the sleep-wake schedule alone is inadequate in effecting large, rapid phase shifts.

It was discovered that bright light is necessary to rapidly achieve phase modification. Dimmer light, such as ordinary indoor lighting on the order of 100-300 lux, was ineffective to cause phase modification which could be clearly attributable to the application of such light. However, when bright light, on the order of 7,000-12,000 lux (optimally averaging about 9,500 lux or greater in the preferred embodiment) is applied daily, phase shifts on the order of 9-11 hours in a 2-3 day period are commonly observed. (For intuitive reference, 9,500 lux is equivalent to the outdoor illumination near the time of dawn or dusk. Bright sunlight at noon presents an ambient light intensity of approximately 100,000 lux.) As can be seen in FIG. 9A, displacement of darkness/sleep alone 6 hours later in time--as will often be required of shift workers or transmeridian travelers--does not result in an appreciable shift of circadian phase position. However, exposure to a bright light stimulus of appropriate intensity at an appropriate phase concurrent with the same displacements of darkness/sleep (FIG. 9B) results in a rapid and large (7.5 h) shift of circadian phase position. Although the circadian timing system would eventually adapt to a shift in the timing of the darkness/sleep schedule, use of the bright indoor lights in conjunction with the shift accelerates the rate of adjustment by 2-5 fold.

B. Bright light can reset rapidly the phase of the human circadian pacemaker independent of the timing of the sleep-wake cycle.

As shown in FIG. 10, during the first endogenous circadian phase (ECP) assessment, the subject's ECP temperature minimum (as indicated by the encircled X) was misaligned from the timing of his sleep-wake cycle, occurring 8-9 hours later than normal at 4:10 p.m. The subject's scheduled sleep/darkness episode was held essentially constant, and the subject's ECP temperature minimum remained essentially unchanged. Then, independent of the timing of the scheduled darkness/sleep episode, a bright light stimulus was introduced (large open boxes) which rapidly reset the circadian pacemaker to a normal phase position, with the ECP temperature minimum occurring 2.25 hours before the subject's waketime of 9:00 a.m.

For any given light-dark/sleep-wake schedule, it has also been discovered that the magnitude of the phase shift is critically dependent on the timing of onset of the bright light pulse with respect to the preexisting circadian cycle. Not only the magnitude, but also the direction (advance or delay) of the phase shift can be drastically affected by this pulse onset phase. A time of particular sensitivity to bright light has been found to be in a time frame approximately two-three hours before and after the endogenous circadian pacemaker minimum. Small changes in the phase of application of light pulses can make the difference between subsequently advancing, or delaying, the circadian cycle by several hours. This observed result accentuates the necessity for an accurate method of assessment of the existing circadian phase.

C. For any given light-dark/sleep-wake schedule, the magnitude of the phase shift which can be achieved in response to bright light depends on the phase of bright light administration with respect to the phase of the circadian pacemaker (as marked, for example, by the endogenous component of the body temperature cycle). FIG. 11 presents the raw data from our experiments using the technique for evaluating circadian phase capacity measuring the amount of phase shift achieved in response to bright light stimuli delivered at a range of circadian phase positions with respect to the ECP temperature minimum.

FIG. 12 presents an average plot of the same data as plotted in FIG. 11. However, data points in the advance and delay zones have been binned and averaged across intervals of three hours' duration. Vertical bars represent the standard error of the mean. In those bins which contained less than four values, a dashed line has been used to approximate the mean. Standard errors were not calculated for these bins.

The shape of this response curve to light suggests that the phase marker we have chosen--the ECP temperature minimum and its correlates--does indeed reflect the phase position of the human circadian pacemaker since the response curve generated using this phase reference marker shares the expected properties of phase delays in the early part of the subjective night, phase advances in the late subjective night and a zone of relative insensitivity during the subjective day.

Since the phase response curve is a circadian pacemaker property, the phase reference marker which we have chosen (i.e., the endogenous component of the core body temperature rhythm) must maintain a relatively fixed phase relationship to the output of the circadian pacemaker. (See S. Dean and C. S. Pittendrigh, "A Functional Analysis of Circadian Pacemakers in Nocturnal Rodents: II. The Variability of Phase Response Curves," J. Comp. Physiol., Vol. 106, pp. 253-266 (1976).)

The magnitude of the shifts and shape of the response curve (see A. T. Winfree, The Geometry of Biological Time, Springer-Verlag, (New York, Heidelberg, Berlin), 1980, pp. 36-38, p. 53), unexpectedly indicates that our three pulse protocol has generated what is called a strong "Type 0" phase response curve, usually observed only in plants and insects in response to light and seldom observed in mammals or other higher organisms (see D. S. Saunders, An Introduction to Biological Rhythms, Blackie (Glasgow and London), 1977, pp. 40-64). The existence of Type 0 resetting means that a full description of the state of the oscillator requires amplitude as well as phase of the oscillator. Furthermore, for Type 0 resetting, there is at least one point on the resetting curve for which the amplitude of the oscillation passes through zero during the resetting process, and that for a correct phasing of the stimulus and adjustment of its strength, zero amplitude can be achieved. The phase response curves to light found in most mammals, including primates (see T. M. Hoban and F. M. Sulzman, "Light Effects on Circadian Timing System of a Diurnal Primate, the Squirrel Monke," Am. J. Physiol., Vol. 249, pp. R274-R280 (1985)) are of a weak "Type 1" resetting pattern, which are generally of low amplitude (maximum phase shifts of only one to three hours) and do not have a sharp "break point" between the advance and delay portions of the curve. Type 1 resetting can be described in terms of phase only, whereas for Type 0 resetting to be described fully, both amplitude as well as phase must be considered.

Therefore, this empirical finding of Type 0 resetting in humans in response to scheduled episodes of bright light and darkness would not have been predicted a priori by someone skilled in the art and knowledge of the subject. This information makes possible many of the useful applications described herein.

Referring to FIG. 11, the effect of the timing of application of bright light pulses on the circadian phase shift is illustrated. FIG. 11 comprises two time axes superimposed on one another. The top time axis is determined by the placement of the endogenous circadian pacemaker minimum at 302, labeled ECP_(min) (Endogenous Circadian Phase minimum). The bottom time axis presents a standard 24-hour day in a way which associates the endogenous circadian phase minimum with a time of 6:00 a.m., as indicated at 304. The plotted points are experimental results of repeated use of the Method of Assessment of Circadian Phase and Amplitude Resetting Capacity, described above. Data points above the zero phase change line 310 indicate phase advances. Data points below the zero phase change line 310 indicate phase delays, measured after the application of bright lights. The independent variable in each of these experiments was the time when, in the existing endogenous circadian pacemaker cycle, the bright light pulse began.

The distribution of data points in FIG. 11 illustrates that there is an interval of particular sensitivity around the minimum of the deep circadian pacemaker. Points generally indicated at 306 show a phase advance, while points generally indicated at 303 show a phase delay. The relatively small phase separation of the pulse onsets for different experiments, as well as the strength of the resultant phase changes for pulse onsets timed closely together, accentuate the necessity for careful timing of the light pulses. Application of bright light pulses several hours before or after the endogenous circadian phase minimum result in more modest phase delays as indicated at 312.

Results such as those found in FIG. 11 are consistent with the Phase Response Curve (PRC), described above and shown to have general validity during the "subjective night" of lower animals. However, earlier PRC's did not take into account the importance of the timing of episodes of darkness and ordinary room light.

Unfortunately, a 2-dimensional PRC cannot take into consideration the importance of the scheduling of episodes of darkness (rest) in relation to the bright light pulse applications. FIG. 14 demonstrates how proper alteration of episodes of darkness allows more control to be exercised over the change in circadian phase, particularly in the zone of greatest sensitivity (i.e., breakpoint).

Resetting Response is Phase Dependent

The magnitude and direction of the phase shifts induced by a three-cycle light stimulus are dependent upon the initial endogenous circadian phase at which the light exposure occurs (FIG. 15B described in greater detail below). The largest phase shifts are observed when the light stimulus occurs during the "subjective night," reaching a maximum when the midpoint of the light stimulus is centered on the initial ECP_(min) (relative clock hour, 05:00).

Advances to an earlier phase tend to occur when the light stimulus is centered late in the subjective night, after the initial ECP_(min), while delays to a later phase occur when the light stimulus is centered early in the subjective night, before the initial ECP_(min). Only small shifts are observed when the center of the light stimulus occurs within the subjective day (i.e., 11:00 to 19:00 initial relative clock hour).

These findings demonstrate that the timing of light exposure is a critical determinant of the magnitude and direction of the resetting response of the human circadian pacemaker to light. These results are consistent with the general properties of phase response curves to light described in all other species, including primates, although the class of this response curve (Type 0) has very rarely been observed in vertebrates and was certainly unexpected in humans.

Furthermore, these results support the use of the endogenous circadian temperature cycle as an accurate reference time scale for deriving the relationship between the time of stimulus administration and the phase resetting response of the endogenous circadian pacemaker in human subjects, analogous to the established use of the free-running rest-activity cycle as a reference time scale in lower organisms. Paradoxically, for reasons discussed above, the free-running rest-activity cycle itself does not appear to provide a comparable reference time scale in humans; in fact, a recent study attempting to use the human rest-activity cycle to assay circadian phase resetting in response to bright light exposure was apparently unable to demonstrate the phase-delay capacity revealed by our data.

The bright light pulse applications according to the present invention may be facilitated through use of many different types of commercially available lamps, for example, ordinary fluorescent lights. Because the photopic and scotopic sensitivity functions cover most regions of the visible spectrum, it is likely that most "white" light and many monochromatic bands of light could be used effectively, provided luminous flux is sufficiently great in the range of the pertinent visual sensitivity function.

In many of our studies we have used Vitalite fluorescent sources (Duro Test Corp.) which have a spectral output designed to mimic sunlight, including UV light. We have also, however, used commercially available cool white fluorescent sources in other studies, and have seen no difference in effect at the same illuminance level. In addition, we have employed goggles which shield subjects from UV light exposure and we have seen no difference in resetting response at the same illuminance level. Fluorescent lamps were chosen over incandescent lamps for primarily economic reasons. As stated previously, there is no reason to suppose superiority or inferiority of a particular lamp at the appropriate light intensity as measured in lux or foot-candles, which are weighted to reflect the human visual sensitivity function.

Bright light may be administered by any means which provides adequate optical illumination, and it is recommended that user comfort, safety and practicality be considered. Nevertheless, to achieve the lighting intensity desirable for practice according to the preferred embodiment of the present invention 7,000-12,000 lux, averaging about 9,500 lux, essentially the entire ceiling (or wall, etc.) of a room must be covered with fluorescent light fixtures if the subject is to be allowed to freely move throughout the room. Other devices, such as portable goggles or helmets or other appliances may also be employed. Such devices will be explained in greater detail below. All that is necessary is that the retina be exposed to bright light for the properly chosen pulse duration. Of course, the subject need not be staring directly at lights. It is sufficient that he be effectively surrounded by light of the appropriate intensity for the appropriate duration.

D. Although application of bright light pulses can alone cause rapid phase modifications, the timing of episodes of darkness (rest) with respect to the bright light pulses also has a profound effect. Together, a schedule of bright light pulses and periods of darkness or diminished light maximizes the efficiency of the phase modification.

One of the most unexpected empirical results of the studies conducted to form a basis of this invention is the importance of darkness/sleep in determining the phase shift elicited in response to a bright light stimulus at a given phase. The upper panel of FIG. 13 illustrates a subject with an ECP temperature minimum occurring at its normal position, just prior to the end of the daily darkness/sleep episode. Exposure to bright light each morning for three consecutive days resulted in a small phase advance of the ECP temperature minimum, such that it now occurred 2.0 hours before the subject's habitual waketime.

However, as shown in FIG. 13B, daily exposure to the light at the same relative phase position concurrent with a phase advance of the daily episode of darkness/sleep resulted in a marked phase advance of the circadian phase position during the same interval. This demonstrates the importance of the timing of darkness/sleep in determining the magnitude of the phase shift induced by bright light. Thus, scheduling the timing of the daily episode of darkness/sleep is a critical element in the successful implementation of this invention because of its governing effect over the magnitude of the response to the stimulus at certain phases of administration. This governing effect of the scheduling of darkness/sleep on the magnitude of the response to bright light is opposite to that which previously would have been predicted by one skilled in the art, since it was thought that humans were insensitive to light intensities typical of ordinary indoor room light (100200 lux) (see A. J. Lewy et al Immediate and Delayed Effects of Bright Light on Human Melatonin Production: Shifting `Dawn` and `Dusk` Shifts the Dim Light Melatonin Onset (DLMO)," Annals NY Acad. Sci., pp. 253-259, (1985)).

FIG. 14 illustrates the overall importance of the timing of darkness/sleep in determining the phase shift response to bright light, regardless of the circadian phase of bright light administration. The response elicited is plotted with respect to the interval between the end of the darkness/sleep episode and the ECP temperature minimum. FIG. 11 and FIG. 14, when considered together, provide an adequate description of human phase resetting capacity to schedules comprised of bright light, ordinary indoor room illumination, and darkness, where corresponding data points in the two figures can be identified on the basis of the phase shifts achieved. The schedule preferred to induce any phase shift desired can be derived from those two figures, as will be illustrated in the section below entitled: "Phase and Amplitude Modification Using Empirical Foundations."

E. The timing of absolute darkness/sleep can determine the erection of the phase response to bright light in humans, even when the bright light stimuli are administered at the same circadian phase.

The upper two panels of FIG. 15 illustrate in a different subject the same type of magnitude governing effect of darkness/sleep position on the circadian phase-resetting response to bright light as that illustrated in FIG. 13 and described in Section D above.

However, the third panel of FIG. 15 illustrates that if the timing of the darkness/sleep episode is scheduled to immediately follow rather than precede the daily bright light exposures, a substantial phase delay shift is elicited rather than the phase advances generated by the prior light exposures given at the same relative phase position. This effect of the scheduling of darkness/sleep vs. the scheduling of ordinary indoor room lighting is in sharp contrast to the predictions which had been made earlier by those skilled in the art (see S. Dean and A. J. Lewy, "Scheduled Exposure to Daylight: A Potential Strategy to Reduce `Jet Lag` Following Transmeridian Flight," Psychopharmacol. Bulletin, Vol. 20, pp. 566-568, 1984), since it had been hypothesized by Lewy and others that the physiologic response of the circadian timing system to light only occurred when the light intensity exceeded the "threshold" intensity (about 500 lux) required to suppress the secretion of the hormone melatonin by the pineal gland. According to such earlier hypotheses, exposure to subthreshold levels of light intensity--whether total darkness or the 100-300 lux intensity of ordinary indoor room light--were both ineffective as compared to brighter light exceeding the 2,500 lux required to substantially fully suppress melatonin production.

Strong (Type 0) Resetting in Human Subjects

The magnitude of the observed phase shifts and the shape of the response curve derived from them (FIG. 15B) indicate that a standard three-cycle stimulus has unexpectedly generated what Winfree has termed strong "Type 0" circadian phase resetting.

The details of FIG. 15B are next described.

FIG. 15B illustrates phase dependent resetting responses of the human circadian timing system to light exposure. Resetting responses are plotted with respect to the initial circadian phase at which the brightness-weighted midpoint of the overall light stimulus occurred (φ_(i)). In the upper abscissa, initial ECP_(min) =05:00); in the lower abscissa, initial ECP_(min) =0. The solid line represents the model according to a preferred embodiment of the present invention fit to the data as formatted in (C), which has then been projected onto (A) and (B).

Plot (A) illustrates human phase-response curve induced by exposure to the 3-cycle light stimulus. The stippled (dotted) area indicates the initial subjective night. Note that when the data are plotted in this standard format, there is an artifactual discontinuity, or "break point", in the curve during the subjective night where small differences in the initial circadian phase of the light stimulus appear to reverse the direction of the resulting phase shift. That the data is in fact continuous is revealed below.

Plot (B) illustrates data from (A) are replotted in monotonic format with the same abscissa, but with an ordinate which represents the number of hours between the post-intervention ECP_(min) and the pre-intervention ECP_(min), t₂ -t₁ (=-Dφ). Remaining symbols are as in (A). This projection reveals that there is not a true discontinuity in the phase response curve.

Plot (C) illustrates human phase-transition curve to the 3-cycle light stimulus. Data are replotted in a format introduced by Winfree. Abscissa as in (A) and (B); left ordinate is φ_(f), where φ_(f) =(φ_(i) +Dφ) _(modulo) 24 h. In the right ordinate, relative clock hour is defined with respect to the final ECP_(min) (05:00=final ECP_(min)), rather than the initial ECP_(min). Therefore, in (C) the stippled area represents the final subjective night. Note that there is an excluded zone during which final ECP_(min) never occur as a result of exposure to the light stimulus. The average zero slope of the data curve in (C) indicates that the stimulus induced Type 0 resetting, as defined by Winfree.

Using non-linear least squares, the mathematical model according to a preferred embodiment of the present invention was fit to the data in (C). Estimated parameters and their standard errors are: a=11.06±0.3; φ_(c) =0.05±0.01; a=0.70±0.1; b=0.45±0.13; covariance (a,b)=-0.01. Linear transformations of these variables yield the following estimates of the light sensitivity parameters: (a+b)=1.15≡0.06 (maximal effectiveness); (a-b)=0.25±0.23 (minimal effectiveness).

As shown in FIG. 15B, both phase delays and phase advances of up to 12 hours were observed in response to the stimulus. In fact, in that region of greatest sensitivity, small changes in the phase of stimulus administration were associated with substantial changes in the magnitude and apparent direction of the response (i e., from maximal phase delay to maximal phase advance), although the artifactual discontinuity in Panel A is resolved when the same data are replotted in Panel B. These characteristics are all typical of strong Type 0 phase resetting.

This is in contrast to weak Type 1 resetting, in which there is no break point in the phase response curve (as there is in Panel A). On the contrary, resetting responses are minimal at the inflection point between phase delays and phase advances in Type 1 resetting.

A plot of final versus initial phase of the light stimulus (φ_(f) versus φ_(i), as shown in Panel C) confirms this conclusion, since its average slope of 0 represents, by definition, strong Type 0 resetting. This indicates that our standard stimulus was strong enough to reset the human circadian system by an amount sufficient to transform the time at which the bright light exposure occurred into the subjective day, regardless of the initial phase (φ_(i)) at which that stimulus was applied (subjective day or subjective night). Consequently, all the final phases (φ_(f)) at which the light stimuli occurred were limited to the subjective day, leaving empty a 10-hour zone surrounding the subjective night (stippled area in Panel C).

The demonstration of Type 0 resetting in human subjects indicates that exposure to light affects not only the phase of the human circadian pacemaker but also its amplitude of oscillation. This is consistent with our recent observation that exposure to bright light can enhance or suppress endogenous circadian amplitude, depending on the phase at which the light exposure occurs.

Previously, strong Type 0 resetting has been reported primarily in plants and insects, whereas weaker Type 1 resetting has been considered characteristic of higher organisms. In fact, the house sparrow (Passer domesticus) is the only vertebrate in which Type 0 resetting by light has previously been reported, although Gander's data on the Polynesian rat (Rattus exulans) support the notion that mammals are capable of Type 0 resetting in response to an extended (8 or 16 hour) light stimulus.

The belief that higher organisms are relatively insensitive to light probably stems from the fact that the classical studies which formed the basis of circadian phase resetting theory happened to be carried out on an unusually light-sensitive circadian rhythm, pupal emergence in Drosophila pseudoobscura. Those pupae are so exquisitely sensitive to light that a mere 55 seconds of exposure to a dim blue light (1 W/m²) results in strong Type 0 resetting of the circadian pacemaker gating that critically timed event. However, it was more recently found that adult flies of the same species require 12 hours of exposure to 7,000 lux of white light to achieve comparable Type 0 resetting of their circadian activity rhythm. Furthermore, the cockroach Leucophaea maderae requires exposure to 80,000 lux of light for 12 hours to achieve strong Type 0 resetting of its locomotor activity rhythm, indicating that there is a wide range of light sensitivity, even among insects.

Therefore, although it has been suggested that, compared to other organisms, humans are very insensitive to phase resetting by light, our data indicate that the responsiveness of the human circadian pacemaker to light is, in fact, within the range observed in other species. Additional studies are now needed to determine the strength of the light stimulus necessary to induce strong Type 0 resetting in other diurnal mammals.

F. Not only the phase, but also the amplitude, of the deep circadian pacemaker is affected by the application of bright light pulses.

By reducing the amplitude of oscillation with a first pulse or sequence of pulses, the effect of any subsequent pulses on phase shifting is enhanced. In the extreme case, when the amplitude is reduced to zero, a subsequent pulse of light or darkness can immediately reset the deep circadian pacemaker to a predefined phase. In the development of the methods described herein we have discovered that the amplitude of the endogenous temperature rhythm, measured by the Constant Routine method, serves as a useful marker of the amplitude of the output of the endogenous circadian pacemaker.

One of our elderly subjects, shown in Panel D of FIG. 7, had a core body temperature recording during a 40-hour endogenous circadian phase (ECP) assessment which revealed an absence of any detectable circadian variation. Likewise, cortisol secretion revealed no evidence of rhythmicity.

In order to determine whether the lack of circadian variation in that subject's Constant Routine temperature recording reflected a reduced output of the circadian pacemaker, we conducted a follow-up recording for six weeks in a time-isolated environment, which confirmed the original finding and revealed a distinctive pattern in which the subject free-ran with an activity-rest cycle period which was alternatively shorter or longer than 24 hours (about 22 and 27 hours, respectively) (FIG. 16). Analysis of the clustering of bedrest episodes suggested the possibility of a weak output of the endogenous circadian oscillator at a period of 23.7 hours, which was further supported by the presence of a low amplitude temperature oscillation during his final constant routine, although bedrest episode durations were not consistently related to the phase of that cycle and non-parametric spectral analysis of temperature did not show a prominent peak at that or any other period (FIG. 17).

The very abnormal free-running activity-rest cycle pattern of this subject, who had a markedly reduced temperature cycle amplitude during his screening ECP evaluation, suggests that in his case the endogenous circadian oscillator had a substantial reduction in output as compared to the average subject. Otherwise, his unprecedented activity-rest cycle periods during desynchrony of first 22, and then 27, hours (activity-rest cycle periods which have not been seen in healthy young subjects, (see R. Wever, The Circadian System of Man, Springer-Verlag, New York, (1979)), would have been captured into synchrony by presumably near-24-hour output of the endogenous circadian oscillator. Thus, the body temperature cycle amplitude during the ECP protocol was an accurate assessment of the amplitude of the output of the circadian pacemaker.

The confirmation of our hypothesis that the core body temperature pattern reflected the output of the endogenous circadian pacemaker has led us to conclude that interventions which change the amplitude of the endogenous component of the temperature cycle may well be altering the output of the circadian pacemaker. The phase and amplitude resetting assessment technique which we developed thereby allows us to assess the effects of a particular intervention on the amplitude, as well as phase, of the circadian pacemaker.

We have learned several general principles in the development of this method for amplitude modification. First, certain lighting regimens can reduce the amplitude of the endogenous circadian pacemaker, and in certain experiments have reduced the amplitude to a level indistinguishable from zero. Such reduction in circadian amplitude is associated with a decrease in the range of a variety of circadian controlled variables, and is especially useful in averting the decrements in physical and cognitive performance associated with the trough of the circadian temperature cycle. Also, such reduction in amplitude may facilitate the rapid shifting of circadian phase by means of manipulation of lighting schedules; and as noted above, it has been reported by Reinberg that persons with certain amplitude characteristics are better suited to the demands of shift-work. Likewise, certain lighting regimens can increase the amplitude of the endogenous circadian pacemaker, which should facilitate both greater daytime alertness and deeper sleep at night.

Data on which the present invention is partially based are therefore inconsistent with the notion that light must exceed a certain threshold to have an effect on the circadian system, such as 500 lux, as has been suggested. The traditional "phase response curve", derived principally from brief light pulse experiments conducted on organisms living in otherwise constant darkness, is only a partial description of human phase resetting responsiveness to light-dark cycles.

The present invention uses a more useful description of circadian phase resetting by light in humans. This description requires a phased summation of graded responses. That is, the response of the circadian system to a given light-dark schedule depends on the cumulative effect of all the light intensity transitions within that schedule, and that the range of intensity changes which exert an important effect are not limited to bright light (e.g., greater than 2,000 lux) but encompass a graded range of responses to light exposures occurring from zero light intensity (i.e., darkness) to over 100,000 lux (e.g., the ambient light intensity of the midday sun).

These findings are verified by several clinical intervention studies and demonstrate the practical use of the above principles in the treatment of actual jet-lag and sleep disorders. The utility of the above principles in the treatment of age-related changes in circadian function, and in the facilitation of temporal adjustment typically required by shift-workers, are also demonstrated.

Influence of Ordinary Indoor Room Light

G. The phase shifts induced by a stimulus are dependent not only on the timing of exposure to bright light, but also on the timing of exposure to ordinary indoor room light.

As is illustrated in FIG. 15A, we found that changes in the timing of exposure to ordinary indoor room light (averaging 150 lux) can have an effect on the magnitude and the direction of a phase shift induced by a bright light stimulus given at a time of peak light-sensitivity.

FIG. 15A illustrates daily illuminance patterns and resulting phase shifts in three different trials of light exposure in a 22-year-old man. In each of these trials, the midpoint of the bright light exposure (t_(BL)) was scheduled to occur at approximately the same initial ECP_(min) (t₁, indicated by a vertical dashed line), while the timing of exposure to room light (and therefore darkness/sleep) was varied.

In (A), exposure to room light occurred predominantly after the bright light exposure, whereas in (C), most of the exposure to room light occurred before the bright light exposure. In (B), the midpoint of the room light exposure (t_(RL)) was concurrent with that of the bright light exposure (t_(BL)). While t_(BL) occurred at a relative clock hour of 05:20 (±15 minutes) in all three cases, the relative clock hours at which the midpoints of the overall light exposures occurred (t_(L), which is a brightness weighted average of t_(RL), as described herein) were 06:36, 05:34, and 3:43 for (A), and (B) and (C), respectively. These t_(L) values correspond to initial circadian phases at which the stimuli occurred (φ_(i)) of 1.6 hours, 0.6 hour, and 22.7 hours, respectively.

These differences in φ_(i) were associated with marked differences in the magnitude and direction of the resetting response to the light stimulus (Dφ for (A)=+3.6 hours; for (B)=+8.6 hours; and for (C)=-5.9 hours), consistent with the results discussed below (in FIG. 15B, Panel A). These data indicate that the timing of exposure to room light can substantially modulate the phase-shifting effect of bright light when t_(BL) occurs at (or near) the most light-sensitive phase.

These results are not consistent with the notion that the human circadian timing system is unperturbed by exposure to ordinary indoor room light of an intensity below the threshold required for melatonin suppression. Thus, suppression of circulating melatonin levels by bright light exposure does not appear to be required to perturb the human circadian pacemaker, suggesting that light acts directly on that pacemaker, probably via the monosynaptic retinohypothalmic tract in humans. This conclusion is consistent with data from Orth and Island, who reported twenty years ago that experimental alterations in the timing of indoor room light could shift the phase of the plasma 17-hydroxy-corticosteroid cycle in human subjects, even when the timing of sleep was held constant. However, this does not preclude an influence of either the rest-activity cycle or pineal melatonin secretion on the entrainment process, as recent evidence has suggested.

As described above, bright light can shift the phase of the endogenous circadian pacemaker, even when the timing of the sleep-wake schedule is held constant. However, in some studies, the influence of ordinary indoor room light on the response to bright light exposure cannot be unambiguously ascribed to laboratory light, since the subjects slept during scheduled dark episodes. Thus, the influence of exposure to room light could conceivable due in part to an internal effect of the rest-activity cycle on the pacemaker, such as has recently been described in animal studies (N. Mrosovsky and P. A. Salmon, Nature 330, 372 (1982)).

However, free-running endocrine rhythms with an intrinsic period as low as 24.35 hours have been reported in blind subjects whose rest-activity cycles are constrained to 24 hours, indicating that the range of entrainment of those rhythms to the rest-activity cycle in those blind subjects is less than 0.35 hours. The range of entrainment for such rhythms is 3 times larger (about 1.2 hours) in normally sighted subjects whose rest-activity cycle is similarly constrained to 24 hours, but who are also exposed to a concurrent cycle of ordinary indoor room light and darkness (J. E. Fookson et al., Sleep Res 13, 220 (1984)). Internal (non-light) effects of the rest-activity cycle thus probably contribute no more than about 30 percent of the total entraining effect of the imposed schedule of ordinary indoor room light and darkness/sleep.

Therefore, the timing of exposure to both bright light and ordinary room light have been incorporated into the definition of the stimulus and the evaluation of its phase-resetting response, according to the principles of the present invention. Methods according to the present invention account for both light levels by averaging the midpoint of exposure to bright light with that of room light, using a formula which includes an approximately weighting ratio of their relative importance. The phase of that brightness-weighted midpoint of the overall light exposure is used here to denote the initial circadian phase, φ_(i), at which the light stimulus is applied.

The phase of the overall light exposure was estimated by calculating a brightness-weighted average, t_(L), of the midpoint of the 5-hour exposure to bright light (7,000-12,000 lux), t_(BL), and the midpoint of the 16-hour exposure to ordinary indoor room light (100-200 lux), t_(RL). By comparing the results of resetting in which the midpoints of the bright light and ordinary room light exposures were coincident with trials in which they were not, we have found that the circadian phase of bright light exposure is the dominant factor determining the magnitude and direction of the resetting response.

In fact, small displacements of φ_(i) due to changes in the timing of room light can only have a critical effect when φ_(i) is at the very steepest point on the response curve (i.e., at the ECP_(min)). Nonetheless, t_(L) can be estimated using the formula:

    t.sub.L =(k)t.sub.BL +(1-k)t.sub.RL

where

t_(L) is the brightness-weighted midpoint of the overall light pattern,

t_(BL) is the midpoint of bright light, and

t_(RL) is the midpoint of room light.

A working estimate of the weighting ratio (k)/(k-1) is 2.7.

Of course, an enlarged set of experiments would be desirable to estimate that weighting ratio with greater precision. In any event, the phase-resetting curve derived from our data using

    φ.sub.i -(t.sub.BL -t.sub.1).sub.modulo 24 h

is qualitatively the same as that derived using

    φ.sub.i -(t.sub.L -t.sub.1).sub.modulo 24 h'

since the average difference between the actual value of t_(BL) and that calculated for t_(L) was only 0.66 hours for the resetting trials reported here.

4. Phase and Amplitude Modification Method Using Empirical Foundations

The modification method according to the present invention is premised on the observations that bright light has a direct effect on the endogenous circadian pacemaker, and that the effect of the bright light is significantly enhanced by proper scheduling of dark (rest) episodes. Further, proper application of light pulses and darkness episodes control the amplitude of the endogenous circadian pacemaker even to the point of reducing the amplitude to zero, so that subsequent exposure to an episode of light or darkness may immediately reset the endogenous circadian pacemaker to a desired phase.

Whereas phase shifts induced by a 3-cycle stimulus are approximately equivalent to those induced by a 7-cycle stimulus, the endogenous circadian temperature amplitude observed after administration of the 3-cycle stimulus is, on average, 12.8 percent lower than its normal value (of 0.5 degrees C.) after substantial (>4 hour) phase shifts. Pilot studies indicate that the final circadian phase (φ_(f)) is not changed by an additional (4th) cycle of exposure, even if the first 3 cycles had induced substantial phase shifts. However, that extra cycle does normalize amplitude.

This, together with our data from the 7-cycle trials, suggest that post-stimulus phase transients (C. Pittendrigh, V. Bruce and P. Kaus, Proc Natl Acad Sci USA 44, 965 (1958)) are largely complete at the time of the post-intervention endogenous circadian phase assessment.

On the other hand, it does not appear that the observed phase shifts are induced solely by the first exposure to bright light, since omission of the bright light episodes during the second and third cycles does not yield a comparable result to that of our 3-cycle stimulus. These experimental results are consistent with the predictions of the preferred mathematical model, which indicates that a stable phase position should be achieved at all phases (including a full 12-hour phase shift) after the first 3 cycles. Stable phase positioning after phase shifts of less than 12 hours may be achieved in less than three cycles.

A further factor determining of the number of cycles of stimulus needed to cause stabilization of phase positioning is the duration of the stimulus. Generally, longer stimuli (intelligently timed) cause more rapid completion of the shifting and stabilization process.

For the purposes of research, it is advantageous to employ a standard stimulus consisting of three cycles of exposure to a daily illuminance pattern of bright light, ordinary indoor room light, and darkness. Fewer than three cycles of exposure may induce qualitatively different results, including substantial reduction of circadian amplitude.

However, in a treatment scenario (as opposed to an initial research scenario), the introduction of a reduction in amplitude may be permissible, or even desirable. Thus, although some of the results reported in this Specification may comprise 3-stimulus interventions, it is to be understood that treatment methods according to the present invention may comprise interventions of greater or lesser number of repetitions, and/or of different stimulus intensities or durations. Such variations on the actual methods shown in this Specification, and in other interventions not specifically included due to considerations of brevity, lie within the contemplation of the present invention.

The use of empirical results reported here and in literature derived from the work of the inventors, as well as using the mathematical model of the deep circadian pacemaker according to the preferred embodiment of the present invention, allows those skilled in the art to design and implement treatment protocols to achieve clinically desirable results in a variety of situations even though each such situation may not be specifically enumerated in this Specification.

Preferred embodiments of the method for shifting circadian phase based on application of light pulses, and on timing of episodes of darkness (rest) will first be described. Then, application of these methods to particular work schedules, traveling schedules, and circadian phase-related disorders will be presented. Finally, the methods of modifying the amplitude of the deep circadian pacemaker will be explained.

Although the empirically derived procedures for modifying phase and amplitude have been found experimentally to be optimal, for a particular individual in a given circumstance one of the empirically derived regimens may be inconvenient. A computer-based model has therefore been developed which allows the formulation of a variety of alternative schedules with alternative dosages, timing and duration of light exposure which will effect the same result. The theoretical foundations for the computer model are described in section 5 below, and the methods to modify phase and amplitude using that model are further described in Section 6 below.

The remainder of the current section (section 4) will therefore address the detailed description of those procedures to modify circadian phase and amplitude which may be derived directly from empirical data which is currently available.

a. Delaying Circadian Phase Using Experimentally Derived Data

Delaying circadian phase is desirable for westward jet travelers, shiftworkers who must rotate to a later shift (i.e., clockwise rotation), and patients with an undesirably advanced sleep phase (i.e., Advanced Sleep Phase Syndrome, typically, but not exclusively, found in the elderly).

Phase delays of 2-11.5 hours have been achieved in 2-3 days' time by appropriately structuring these days' lighting schedules with particular attention to the timing of bright light and darkness.

In order to best design the lighting schedule, one must have knowledge of the initial circadian phase of the person to be treated. This is best achieved by the previously described embodiment known as the Constant Routine. However, it would be acceptable in most cases to infer such phase based on comparisons made to the body of normative phase data such as is contained within this disclosure (FIGS. 3, 4, 5, and 6A, 6B) or in the literature in general.

By subtracting the initial phase from the desired phase, the magnitude and direction of the required phase shift is determined. Then, by interpolation of FIG. 11, the optimum time to begin the administration of a bright light pulse is determined. This bright light pulse is approximately five hours in duration and has a dosage of approximately 7,000-12,000 lux in a preferred embodiment. Light of half intensity may precede and follow this five-hour pulse for approximately 15 minutes.

By interpolation of FIG. 14, the optimum timing of the dark (sleep) pulse is determined. The dark pulse lasts from approximately six to nine hours in a preferred embodiment. The retina of the eye should be appropriately shielded from substantially all light. This can be accomplished most practically by having the individual remain in a dark room, for example, while in bed sleeping. In the preferred embodiment of the technique, all artificial indoor light sources within the room (e.g., electric lamps or other light sources, gas or flame lamps, televisions, etc.) would be switched off and all sources of natural or artificial outdoor light (e.g., sunlight or street lights illuminating the room through window openings, skylights, or other modes of entry should be shielded from the room, using blackout curtains, opaque shades or other appropriate shielding devices. If the individual is unable to remain in such a dark room during the scheduled dark episode, goggles which effectively absorb 90-95 percent of visible light (such as welder's goggles) may be worn or the individual may wear contact lenses with a similar light absorbing property.

At times not specified above, the person being treated should be exposed to light of normal indoor light intensity (ca. 100-500 lux).

The relative timing of exposure to bright light, room light and darkness can also be derived by interpolation of the data in FIG. 15B, using the formula described in Section 3(G) to estimate the brightness-weighted midpoint of the overall light exposure.

This lighting schedule is repeated for three days in a preferred embodiment. Upon completion of this regimen, the desired phase shift will have been achieved. A second Constant Routine can then be carried out if it is necessary to evaluate the phase or amplitude resetting capacity of the individual on that regimen.

FIG. 18 is a raster diagram which indicates how application of bright light accelerates the phase delay shifting of the circadian pacemaker trough much faster than mere manipulation of the activity-rest cycle. FIG. 18 is a raster diagram in which the information on a horizontal time axis, for example, Day 5, contains information about both Days 5 and 6. Similarly, the time axis for Day 6 contains information about Days 6 and 7. Thus, the points indicated at 522 and 524 (FIG. 18) are in fact the same experimental point. The hollow bars in FIG. 18 indicate periods of enforced wakefulness during a Constant Routine, and the solid bars indicate periods of enforced bed rest.

The subject was placed on a schedule of cumulatively repeated phase delays in his activity-rest cycle. During some of these delays, bright light pulses were applied in order to determine the effect of circadian phase delay attributable to the bright light pulses. The phase delay was measured using the Phase Resetting Capacity Assessment Method described above.

The first Constant Routine started before time 502 (FIG. 18). During this Constant Routine, the trough of the deep circadian pacemaker was determined to occur at time 512 (Day 5). In Days 6-9, the subject was entrained to a 24-hour activity-rest cycle. At time 504, a second Constant Routine assessment of the deep circadian pacemaker was performed. As shown at time 514 (Day 10), the deep circadian pacemaker trough (ECP_(min)) was phase-delayed by only 0.9 hours, which is statistically insignificant in light of its accordance with previous results under similar circumstances.

On Day 11, the activity-rest cycle of the subject was delayed by six hours. This delay was enforced from Days 11 to 14. Unlike Days 6-9, during Days 12-14 the subject was exposed to 5.5 hours of bright light on three consecutive nights, as indicated at 526 (FIG. 18). On Day 14, a third Constant Routine was entered. It was determined that the deep circadian pacemaker trough occurred on Day 15 as indicated at time 516. The phase delay between time 514 (Day 10) and time 516 (Day 15) was a statistically significant 7.1 hours. This indicates that the application of bright light pulses on successive nights dramatically shifted the phase of the deep circadian pacemaker by a magnitude which is not explainable either by free-running period or by manipulation of the activity-rest cycle.

Days 15-25 of the experiment basically repeat the procedure of Days 5-15. A 7-hour delay in the enforced activity-rest cycle on Day 16 caused a statistically insignificant phase delay in the deep circadian pacemaker of only 1.9 hours. This phase delay of the deep circadian pacemaker is indicated by the relative times of occurrence of the deep circadian pacemaker troughs at time 516 (Day 15) and time 518 (Day 20).

After another shifting of the activity-rest cycle by 7.5 hours on Day 20, bright light pulses of 5.5 hour duration were applied on Days 21-23. A statistically significant 9.9-hour phase shift in the deep circadian pacemaker is indicated by the relative timing of deep circadian pacemaker troughs at time 518 (Day 20) and time 520 (Day 24/25).

In summary, FIG. 18 graphically demonstrates that the phase-shift of the deep circadian pacemaker in response to bright light pulse applications (minus 7.1 and minus 9.9 hours) is far greater than that (less than 2 hours) explainable either by the free-running period or manipulation of the activity-rest cycle.

FIG. 18A-1 and FIG. 18A-2 shows two raster diagrams which demonstrate that bright light can be used to treat the lack of physiologic adaptation to reoccurring night work which leads to dyssomnia, impairment of performance and increased safety hazards. The study involved several individuals, the data from one of which is shown in FIG. 18A-1 and FIG. 18A-2. Statistical results of plural subjects are represented in FIG. 18B.

The study involved a comparison of a control group (exemplified by FIG. 18A-1) and an experimental group (exemplified by, FIG. 18A-2). The study was designed to emulate a realistic night shift worker as much as possible, in that the individuals actually went home after work, rather than remaining in a laboratory environment. The particular raster diagrams shown in FIGS. 18A-1 and 18A-2 are those of the same subject, taken during studies conducted three weeks apart, the subject thus serving as his own control in this case.

In the Control Study, several nights of sleep were observed and documented, as shown by the dark horizontal bars 501. Then, the circadian phase of the subject during the control study was measured using the Constant Routine, during the period indicated generally as 503. The ECP minimum 505 was determined to occur at 5:22 AM.

The following day, the subject changed from day shift (working 9 AM to 5 PM) to night shift (12 midnight to 8 AM). The control group experienced normal levels of indoor illuminations, as indicated by the dotted block at 507. His ad lib daytime sleep episodes are illustrated by the black bars to the right of box 507.

After working four days of night shift, the control group was again tested to determine the ECP minimum. In this particular subject, the ECP minimum 509 was determined to occur at 6:32 AM, a statistically insignificant phase delay of 1.2 hours.

In contrast, the right panel Intervention Study shows the same subject three weeks later undergoing a similar change from working day shift to working four nights of night shift. As in the control study, several nights of sleep were observed at 501. The ECP minimum 511 was determined to occur at 5:13 AM.

The next night following the determination of the ECP minimum determination, this subject was exposed to bright light (approximately 10,000 lux) for a substantial episode time during his work schedule, indicated as the box 513 containing a radiant circle. During the period when bright lights were applied at work, the subject experienced his scheduled sleep episode shown in black bars to the right of box 513. (The short "nap" on the third day of night was unplanned--not part of the schedule--and is not believed to substantively affect the results of the experiment.)

After the four nights of night shift work, the subject's ECP minimum 515 was again determined using the Constant Routine. The ECP minimum had delay-shifted a significant 9.2 hours to 3:22 PM. This new time of occurrence of the ECP minimum thus occurred approximately 1.5 hours before his new, habitual wake time.

Referring to FIG. 18B, the array of changes in the ECP minima of plural subjects are illustrated. As shown, the Treatment Study consistently showed a phase delay of the ECP minimum into the afternoon, indicating adaptation to the daytime sleeping schedule demanded of night shift workers. In significant contrast, the ECP minima of the Control Study subjects were distributed from a slight phase delay to a medley of small shifts and sometimes inappropriate phase advances. The subjects in the Treatment Study also experienced an appropriate shifting in the phase of cortisol secretion, alertness and performance, confirming the utility of the regimen undergone by the subjects in the Treatment Study (FIG. 18C, panels F through G).

FIG. 18C (panels A through E) indicates that such appropriate shifting of these daily rhythms was not achieved by subjects in the control studies, even on the sixth consecutive night of work.

It is believed that the only substantial independent variable is the level of illumination during the subjects' night work shift, the scheduled exposure to "commuting" light after the bright light, and the enforced darkness during the scheduled periods after arriving home in the morning. A comparison of the Control Study with the Intervention Study in the same subject yields similar results with other subjects in the group (see FIG. 188). The fact that the ECP minimum in the Control Study subjects did not adapt to the new sleep time of the subjects (indeed, in most subjects in the Control Study, the phase actually advanced on the order of 1-2 hours), while the ECP minimum of the subjects in the Intervention Study did adapt to the new sleeping schedule, demonstrates that exposure to bright light during night work, advantageously combined with darkness during day sleep, can induce physiologic adaptation to this inverted work-sleep schedule.

In the present study, it was demonstrated that complete physiologic adaptation occurred in a maximum of four days with the appropriate lighting regimen. However, based on other studies (see, for example, FIGS. 18A-1 and 18A-2), adaptation to a forward-shifting work schedule can apparently be achieved in three days. Furthermore, based on theoretical predictions based on the mathematical model of the human circadian system (described below) such adaptation can apparently be achieved in two days. Thus, the study shown in FIG. 18A does not test the limits of speed of adaptation of the deep circadian pacemaker caused by the inventive methods according to the present invention.

To facilitate the useful application of the present invention in a realistic scenario, the above formulation of the lighting regimen factored in the expected light exposure during the employee's commute home after working night shift in a bright light environment. This formulation involved a planned period immediately after (to the "right" of box 513) during which light at that time of day was experienced.

In a practical scenario, it would be expected that different workers, upon leaving work at, say, 8 AM, would be exposed to different levels and durations of light intensity before they arrived at home to sleep. The differences in level and duration of light exposure after leaving work could cause potentially undesirable effects on the resulting phase shift of the ECP minimum. Because the variations in light exposure due to varied daytime schedules may conceivably occur at times of particular phase-shifting sensitivity (that is, near the ECP minimum), it is desirable to minimize any undesirable phase shifting effect of the potentially haphazard exposures to light which may occur for night shift workers during daytime.

According to a preferred embodiment of the shift work adjustment method according to the present invention, exposing night shift workers to bright lights not only during the latter hours of their night shift (such as 4-8 AM), but also during the earlier hours of their night shift (that is, for the full 12-8 AM shift), a greater control over the positioning of the ECP minimum is achieved. This greater control minimizes the effect of spurious daytime exposures to non-ideal light-darkness patterns.

A conceptualization of why such an exposure to bright light would stabilize the entrainment to night shift work and daytime sleep is better understood with reference to the mathematical model of the circadian oscillator, described in greater detail below. At this point, however, it is sufficient to note that the preferred mathematical model according to the present invention involves the weighted midpoint of total exposure to light over extended periods, such as over periods of days. The model is not limited to those known models which are concerned only with shorter "impulsive" administrations of light.

Through a realistic assessment of an individual's most-likely encountered daytime exposure to light and darkness, or through use of normative expectations of such "leisure time" light exposure, an optimum lighting schedule during working hours can be designed, according to the present invention. Based on expected variations in the leisure time exposure to light, there can be designed into the work time lighting regimen (and, assuming the presence of workers willing to take reasonable measures to darken their daytime sleep environments) periods of imposed darkness, any detrimental effect of any undesirable variations in daytime light exposure can be minimized. Indeed, a "buffer zone" of stability about model "desirable" daytime light exposure regimen can be accommodated to some extent by nighttime lighting regimens.

Both employers and employees can be aided by normative data (and/or by theoretical predictions according to the mathematical model of the present invention) regarding probable leisure-time light exposure patterns of the employer's workers on various shifts. The employer can thus intelligently contribute to the efficiency and productivity of his work force by controlling the lighting during working hours. The employer can also reduce employee discomfort due to shift work adaptation by recommending specific regimens as to how to impose periods of darkness (and perhaps bright light) during non-working hours. The improved sense of physical and mental well-being which accompanies physical adaptation to changing shift work would undoubtedly motivate such employees to follow the recommendations which were based on the normative data and/or theoretical data.

According to the preferred embodiment of the present invention, the total pattern of light exposure is accounted for in the assessment and modification of the circadian phase and amplitude. The consideration of the effect of a total pattern includes consideration of light exposure during not only a single day, but over extended periods of several days. Thus, for workers who regularly work night shift certain days of the week, but must re-adapt themselves to nighttime sleep and daytime activity on non-working days, a weekly regimen of exposure to light and darkness can be designed through use of empirical results or the mathematical model according to the present invention.

FIG. 19 illustrates the effective application of the phase-shifting abilities of bright light pulses according to the present invention to transmeridian travelers. The letters A, B, C, and D indicated in FIG. 19 correspond to the segments so labeled in FIG. 18. Referring to FIG. 19, the laboratory experiment recorded in FIG. 18 can be thought of as simulating a transmeridian trip of intercontinental dimensions. The segments A, B, C and D shown in FIG. 18 correspond to the simulated phase shift which would be required by an individual traveling westward, crossing 6-7 time zones. During segment A (days 5-10), without the aid of properly timed bright light exposure, the endogenous circadian pacemaker of the subject only adjusted to a trip equivalent to that of one from New York to Omaha, despite the fact that he was attempting to shift his rest-activity cycle to an equivalent of Samoan time (6 time zones west of New York).

In contrast, during segment B (days 10-15), a more dramatic phase shift caused by the application of bright light pulses on three consecutive evenings would have successfully adjusted a traveler's endogenous circadian pacemaker by an amount equivalent to a trip from Omaha to Auckland.

Once in New Zealand, the individual again attempted to shift his rest-activity cycle by an amount equivalent to a trip from Aukland, New Zealand to Karachi (7 time zones westward). However, without the aid of bright light exposure, his endogenous circadian pacemaker again only drifted to a later hour during segment C (days 15-20) so that the subject's endogenous circadian pacemaker had effectively only adjusted to the time in Sydney. Thereafter, in segment D (days 20-25), the acceleration of the phase shifting due to three days of bright light pulse applications effectively adjusted the subject's endogenous circadian pacemaker to a trip from Australia to London.

The relatively short time in which these dramatic phase shifts are accomplished with the aid of bright light advantageously coincides with the time at which the excessive sleeping (to compensate for sleep deprivation) would otherwise cease to provide symptomatic relief, as described in the Background of the Invention. Thus, methods of endogenous circadian pacemaker phase shifting according to the present invention allow a viable treatment method for transmeridian travelers in a variety of scenarios. Also, the endogenous circadian pacemaker phase shifting according to the present invention allows viable treatment for shift workers in a variety of rotating or otherwise unusual (from the point of view of a diurnal animal) work schedule. For example, FIG. 18 represents a simulation not only of westward travel, but also of a delay shift in the timing of the sleep-wake cycle required of industrial workers when making the transition from day or evening shift work to night shift work. In the case of FIG. 18, it can be seen that the ECP minima are more strategically chosen so as to be maintained in the episodes of enforced darkness (and presumably sleep). As described above, when the ECP minimum is timed to occur within a sleep episode, the sleep tends to be more efficient, and wakeful activity tends to be more productive.

(1) FIG. 20 depicts a schedule, plotted in double raster format, which is optimally suited for achieving a delay shift of approximately 3 hours. Such a delay would be typically required of travellers flying from New York to San Francisco. This schedule utilizes a protocol which resets circadian phase with little effect on circadian amplitude (i.e., Type 1 resetting). The first solid bar represents the individual's habitual sleep/dark episode (typically occurring from 23:30 to 07:30). On the next day, which could be the day before travel, bed time and wake time are moved an hour later, and approximately 4-5 hours of bright light (at least 7,000-12,000 lux) are administered just prior to the sleep/dark episode. On the following day, which could be the day of travel, bed time and wake time are moved an additional hour and a half later, and approximately 3-6 hours of bright light are administered just prior to sleep. If convenient, the bright light could be administered on the airplane flight while en route. This could fit in quite well aboard evening non-stop flights from New York to San Francisco. Should additional phase delay shift be required, this schedule can be continued. It should be noted that, to have the maximum beneficial effect, the strength and duration of bright light dosage will depend on the amount of light to which the person has been previously exposed during the day. However, if a more acute shift is desired, a schedule employing type 0 (amplitude reducing) phase resetting would be faster.

(2) Eastbound travelers (e.g., Seattle to Paris) or shift workers making the transition from evening shift to night shift are often required to accomplish a nearly complete inversion of their sleep-wake cycle (a shift requiring a 10-12 hour delay or a 10-12 hour phase advance) when they travel from the Orient to many parts of the Western world, or when industrial workers must rotate from day work to night work. When the shift required is 10 hours or greater, it cannot practically be accomplished via Type 1 resetting, since 1-2 weeks would be required before the shift were complete. Therefore, the best strategy is to center the light exposure on the circadian temperature minimum and to schedule the timing of sleep/darkness such that it is most conveniently placed with respect to the industrial work schedule or the new time zone. It should be emphasized that the room used for sleeping should be dark and shield out environmental or artificial light sources.

The potential clinical utility of the inventive method to reset human circadian phase has been documented in a follow-up case study of the elderly subject in panel B of FIG. 7 who was an extreme example of the phase advance of the circadian pacemaker which occurs with advancing age. Panel B of FIG. 7 is a comparison of baseline and constant routine temperature data (solid line) in a healthy, 66 year old woman. These data are superimposed upon normative (±S.E.M., vertical hatch marks) temperature data collected from 29 young, normal subjects on the same protocol. Data from the normal controls are averaged with respect to a nominal reference bedtime of 24:00. The black bar represents her bedrest episode which was scheduled at its regular time. Hatched bar represents constant routine assessment of phase and amplitude. The encircled cross marks the minimum of the fitted endogenous temperature rhythm. Note that the ECP minimum occurred at 11:35 p.m., approximately 5 hours earlier than would be expected on the basis of the normative data. However, this phase advance is not apparent during the night preceding the Constant Routine because of masking effects. The rhythm of cortisol secretion was similarly phase advanced during her Constant Routine. Her marked phase advance was confirmed on two subsequent repetitions of this protocol. This condition is often associated with the early bed and wake times often found in the elderly.

FIG. 21 shows a controlled study in which evening exposure to bright indoor light resets the circadian pacemaker of this subject by about six hours, even while her rest-activity cycle is held fixed. Symbols are as previously described with hatched bars indicating bedrest episodes during ambulatory monitoring. Panel (A) (upper left) shows ECP evaluations before and after entrainment schedule involving exposure to ordinary room light suggest a non-significant drift of the endogenous circadian pacemaker. Panel (B) (upper right) shows a raster plot of body temperature troughs during control study. Horizontal black bars with stippling highlight the specific times and days when body temperature was below the baseline entrained mean. Note the absence of a phase shift during exposure to ordinary room light in the laboratory. Panel (C) (lower left) shows ECP evaluations before and after entrainment schedule as described in A, with the addition of an intervention stimulus with evening exposure to bright indoor light demonstrating a 5.7 hour phase delay shift of the circadian pacemaker. Symbols as in (A). The subject was exposed to bright indoor light (7,000-12,000 lux) between 19:40 and 23:40 each day for seven days. Fifteen minutes of intermediate level light (3,000-6,000 lux) preceded and followed each four hour exposure. Panel (D) (lower right) shows a raster plot of body temperature troughs before and during the intervention study confirming the magnitude of the phase delay shift previously shown in (C).

This apparent phase shift was confirmed by a similar shift in the rhythm of serum cortisol (FIG. 22), another marker of the circadian pacemaker. To align the episodic cortisol secretory patterns before and after invention with bright indoor light, their horizontal time scales have been shifted by six hours. Blood samples were collected while the subject was in ordinary room light (50-250 lux) during Constant Routines performed immediately before and after the intervention. The pattern after the intervention (open circles and dashed line) have been translated six hours to the left along the pre-intervention axis (solid axis), thereby aligning the two waveforms. The plot shows that the intervention did not change the shape of the pattern but phase delayed it by approximately six hours. Furthermore, the data in Panel I indicate that the shift took place within the first 1-2 days of the intervention and did not require the full 7 days.

b Advancing Circadian Phase Using Experimentally Derived Data

Advancing circadian phase is desirable for eastward jet travelers, shiftworkers who must advance their sleep time to an earlier hour, and patients with an undesirably delayed sleep phase (i.e., Delayed Sleep Phase Syndrome, typically but not exclusively found in the young).

Phase advances of 2-11.5 hours have been achieved in 2-3 days' time by appropriately structuring these days' lighting schedules with particular attention to the timing of bright light and darkness.

In order to best design the lighting schedule, one must have knowledge of the initial circadian phase of the person to be treated. This is best achieved by the previously described embodiment known as the Constant Routine. However, it would be acceptable in most cases to infer such phase based on comparisons made to the body of normative phase data such as is contained within this specification, or in the literature in general.

By subtracting the initial phase from the desired phase, the magnitude and direction of the required phase shift is determined. Then, by interpolation of FIG. 11 or FIG. 15B, the optimum time to begin the administration of a bright light pulse is determined. This bright light pulse is approximately five hours in duration and has a dosage of approximately 7,000-12,000 lux in a preferred embodiment. Light of half intensity may precede and follow this five-hour pulse for approximately 15 minutes.

By interpolation of FIG. 14 or FIG. 15B, the optimum time to begin the dark (sleep) pulse is determined. The dark pulse lasts from approximately six to nine hours in a preferred embodiment. The retina of the eye should be appropriately shielded from all light.

At times not specified above, the person being treated should be exposed to light of normal indoor intensity (ca. 100-500 lux).

This lighting schedule is repeated for three days in a preferred embodiment. Upon completion of the regimen, the desired phase shift will have been achieved.

FIG. 1 illustrates an example of an individual being phase advanced using this technique, by an amount of eastward travel equivalent to a trip from Seattle to London. Five hours of full bright light (7,000 to 12,000 lux) exposure was initiated at 6:30 A.M. (with 15 minute transitions of 3,000 to 6,000 lux preceding and following the 5 hour full-bright light exposure), about 1.5 hours before his 8:00 A.M. ECP temperature minimum (as determined by an initial Constant Routine in this case or as could have been surmised from the approximately 9:30 A.M. traditional wake-time of this young man using the normative data of FIG. 5). The individual's daily sleep episode was concurrently rescheduled from his approximate habitual bed/dark time of 2:30 A.M. and his approximate habitual wake/lights-on time of about 9:30 A.M. to occur eight hours earlier from 5:30 P.M. to 1:30 A.M.; as if he had traveled from Seattle to London. Follow-up ECP evaluation revealed that his temperature minimum had phase shifted eight hours. This same type of light/dark lighting schedules could also have been used to phase advance shift factory workers rotating from a schedule requring them to work at night and sleep in the morning to one requiring them to sleep at night and work during the day shift. For such changes in sleep schedule required by rotating shift work schedules, whether they rotate in a clockwise or counter-clockwise direction of shift rotation, exposure of the shift workers to bright lights in the workplace during the last 4-5 hours of the day shift (from about 11:00 A.M. to 4:00 P.M.) may markedly enhance their adjustment to the schedule, raise their daytime alertness, efficiency and performance, improve their sleep at home and reduce their proneness for accidents at work. The exact timing of light exposures to be used for rotating shift workers would depend on the specifics of their work schedule, their working conditions (e.g., amount of exposure to outdoor light at work), their average age and the amount of natural light to which they will be exposed to commuting to and from work. Someone skilled in the art could draw upon the information in FIGS. 11, 14 and 15B, together--if necessary--with the mathematical model described below, to develop a paradigm most suitable for the employees concerned. An alternative strategy may be to reduce the circadian amplitude of shift workers via timed exposure to bright light just prior to shift change transitions, thereby facilitating their adaptation.

FIG. 23 is a raster diagram similar to the raster diagram of FIG. 18. FIG. 23, however, involves not only phase delays, but also phase advances.

As in FIG. 18, hollow horizontal bars indicate periods of wakefulness, and solid horizontal bars indicate periods of enforced bedrest. At times 552, 554, 556, 558, 560, 562, and 564, Constant Routines were entered in order to determine the time of occurrence of endogenous circadian pacemaker minima at 566, 568, 570, 572, 574, 576, and 578, respectively. At various points in this laboratory experiment, bright light pulses of 5-hour duration were applied on three consecutive days at the same time, as indicated at 580, 582, 584, 586, and 588.

The timing of application of bright light pulses, as well as the timing of periods of darkness, modified the phase so as to cause controllable phase advances or delays.

During segment A, the subject was entrained to a 24-hour cycle of darkness and light. During this period of entrainment, it can be seen that the ECP phase advanced by 0.8 hours from 566 to 568. (It is unusual for a human subject to display an intrinsic period, T_(x) of less than 24 hours.) During segments B and C, bright light pulses were applied on three consecutive days, as indicated at 580 and 582, respectively. FIG. 23 clearly shows that the bright light pulse groups 580 and 582 occur substantially after the ECP temperature minima 568 and 570, respectively. As a result of the timing of these bright light pulses, in conjunction with the advancement by approximately 8 hours of the darkness onset, ECP phase advances of 8.2 hours and 7.0 hours, respectively, were observed.

Bright light pulse groups, each of 5-hour duration on three consecutive days, were imposed as indicated at 584, 586, and 588. These three bright light pulse groups were timed to be substantially before the ECP minima at 572, 574, and 576. The timing of these bright light pulses, in conjunction with the phase delays indicated by the right shifting of the periods of enforced darkness in segments D, E, and F, caused phase delays of 3.0 hours, 5.4 hours, and 4.5 hours, respectively.

Referring to FIG. 24, the laboratory experiment recorded in FIG. 23 can be thought of as simulating a transmeridian trip of intercontinental dimensions. The segments B, C, D, E, and F shown in FIG. 23 correspond to the simulated phase shift which would be advantageously experienced by a traveler with the itinerary illustrated in FIG. 24. The 8.2-hour and 7.0-hour phase advances noted in segments B and C would be ideal adjustments to a person traveling from Boston to Nairobi , and then from Nairobi to Auckland. Similarly, the phase delays of 3.0 hours, 5.4 hours, and 4.5 hours, would allow adjustment of people traveling from Auckland to Peking, and then on to Moscow and Greenland.

While it should be recognized that it is not generally desirable to experience the ECP temperature minima during the middle of the day time (which is the case in all the FIG. 23 ECP minima), and whereas it may not be practical for many travelers to expose themselves to pulses of bright light and darkness exactly as indicated, the effectiveness of pulses of bright light and enforced darkness in shifting the ECP temperature minima are clearly demonstrated. Variations on light/dark regimens which are more practical, although perhaps not as efficient, will become clearer upon an understanding of the principles expressed in the remainder of this disclosure. Based on either empirically-derived phase response curves, or upon a mathematical model, the most effective practical light/dark regimen may be designed to fit within a schedule of predefined episodes of darkness and ordinary room illumination.

For illustrative purposes, we give examples of lighting schedules which will facilitate (1) a three-hour delay shift, and (2) a ten-hour delay shift. Consideration has been given both to experimental optimization and practical convenience.

FIG. 25 depicts a schedule, plotted in double raster format, which is optimally suited for achieving an advance shift of approximately 3 hours. Such an advance would be typically required of travellers flying from, for example, San Francisco to New York. This schedule utilizes a protocol which resets circadian phase with little effect on circadian amplitude (i.e., Type 1 resetting). The first solid bar represents the individual's habitual sleep episode (typically occurring from 21:30 to 07:30). On the next day, which could be the day before travel, bed time and wake time are moved an hour earlier, and approximately 4-5 hours of bright light (at least 7,000-12,000 lux) are administered upon waking. On the following day, which could be the day of travel, bed time and wake time are moved an additional hour and a half earlier, and approximately 5-6 hours of bright light are administered upon waking. It should be noted that, to have the maximum beneficial effect, the strength and duration of bright light dosage will depend on the amount of light to which the person has been previously exposed during the day. If convenient, the bright light could be administered while en route. This would be ideal if the bright light could be administered aboard the aircraft on the nonstop daily morning flight from San Francisco to New York. Such light exposure could occur via a specially equipped airplane fitted with a cabin with bright light or via the portable goggle units described below.

A very similar protocol can be used to treat patients with Delayed Sleep Phase Syndrome (DSPS). FIG. 26A illustrates the endogenous circadian phase of a 52-year-old woman with DSPS, a sleep scheduling disorder characterized by sleep onset insomnia and excessive daytime sleepiness in the early morning. The patient was treated with three exposures of morning light, without shifting the time of her scheduled sleep-wake cycle, to determine whether her circadian pacemaker could be phase advanced to an earlier hour without disrupting her habitual sleep time (the protocol is illustrated in FIG. 27). After only three exposures to bright light, her circadian pacemaker was phase advanced by nearly 4 hours, to a position normal for a woman of her age (see FIGS. 26A, 26B and 27), and the patient--who had a greater than 5 year history of DSPS--reported an immediate remission from her debilitating symptoms which had interfered with her ability to carry out her profession.

This approach has been reduced to practice in the following example. FIG. 28A and FIG. 28B show the output of the internal body clock as measured during a Constant Routine from a traveler just after returning from Tokyo to Boston (FIG. 29), before any treatment. Note that he reached the low point of his body temperature cycle (the time of greatest sleepiness, lowest performance and peak accident risk) at about 4:00 p.m. Boston time (lower horizontal axis, FIG. 28A, 28B), and he would have ordinarily been asleep, as shown in FIG. 30, which is a raster plot of his travel schedule during that time. But it was highly inappropriate for Boston, where such a misalignment of phases made it difficult for him to remain awake during the local daytime without using stimulants and difficult to sleep at night without the use of sleeping pills. Instead, this traveler was exposed to three daily pulses of bright light and his daily sleep episode was rescheduled to Boston time. Three days after his return to Boston, when the effects on sleep and daytime alertness of "jet lag" from time zone inversion are typically at their worst, his internal clock was instead completely reset by the treatment, with the peak in his daily temperature cycle occurring where the trough had been (FIG. 29B). He then felt full alert during the local daytime and slept well at night, without stimulants or hypnotics. This same process could be applied to make it easier for shift workers to adjust to night work.

Another of the applications of the present invention is in aiding people on an "ordinary" daytime work schedule who may experience some difficulty in awakening, or who may experience some "grogginess" (or other performance impairment) for some time after awakening.

This difficulty in awakening or early morning performance impairment may be due to the fact that, in a large number of individuals, the period of the circadian cycle exceeds 24 hours. The fact that the length of the cycle exceeds 24 hours causes an effective phase delay of the minimum of the endogenous circadian pacemaker from one day to the next. This phase delay is experienced as a depression in the alertness and performance level even if the individual awakens at the same clock time each day, because the individual is awakening at an earlier subjective physiologic time (nearer the ECP minimum).

The effects of this phase delay can be counteracted by resetting the ECP minimum to an earlier time in accordance with the principles of the present invention. Because the preferred embodiments of the present invention operate based on a brightness-weighted midpoint of total exposure to light, and because the phase-shifting sensitivity of the circadian system is greatest when nearest to the ECP minimum, a preferred application of the present invention involves the application of a bright light "pulse" immediately (or soon) after awakening to contribute to a phase advance of the ECP minimum.

The pulse of bright light is best embodied in an application of light in a room where the individual spends his first time period after awakening, usually (but not necessarily) in the bedroom (e.g., via a luminous, rather than an auditory, alarm clock), or in the bathroom. The placement of a panel of bright lights in or above the headboard of the bed or next to the bed or in the bathroom or shower has the economic advantage that a relatively small number of lights are necessary to achieve the desired level of illumination, due to the small size of the bathroom compared with other rooms in the house. Of course, all that is physiologically necessary is that the desired level of illumination is experienced as soon after awakening as possible (assuming the normal case, that the time of awakening is after the ECP minimum). Any other means of illumination other than a bank of lights in the bathroom thus lie within the contemplation of the invention.

Thus, the present invention envisions a method of entraining subjects to a wakeful daytime schedule and facilitating physiologic optimization to the daytime schedule, the method comprising the steps of allowing the subjects to awaken during a period of time immediately after the minima of their endogenous circadian pacemaker, and exposing the subjects to bright light in a period of time immediately after awaking, whereby the midpoint of the total overall light exposure resets the minima of their endogenous circadian pacemaker to an earlier time, whereby physiologic adaptation of the subjects to a morning wake time is facilitated.

The degree of effectiveness of the method varies with the length of time which the individual spends in a bright light environment, the phase of administration of light (how close to the ECP minimum), the intensity of the light, and the number of light exposures. However, any bright light early in the subjective day tends to phase-advance the ECP minimum at least to some extent, based on its effect on the brightness-weighted midpoint of the total light exposure. This method thus allows a tangible improvement in circadian phase adjustment while minimally encroaching on the individual's normal daytime activities.

C. Reducing Circadian Amplitude Using Experimental Data

Reduction in circadian amplitude is sometimes desirable in order to place the circadian timing system in a more labile position, as would be desired when anticipating a change in circadian phase. This procedure would be desirable for travelers crossing many time zones or the shift worker making a change in worktime. As circadian amplitude is sufficiently reduced, the circadian timing system is correspondingly sensitized to a single day's lighting cycle. Thus, travelers or workers who intend to be exposed to the environmental lighting schedule (or a regimen of indoor bright light exposure designed to approximate environmentally available light) immediately upon assuming their new schedule could benefit greatly from a preparatory reduction in circadian amplitude.

There is a range of amplitude reduction which can be achieved using specifically timed regimens, which optimally include both episodes of darkness and episodes of bright light exposure. It is possible to effectively reduce circadian amplitude to zero in two days of scheduled light exposure.

In order to best design the lighting schedule, one must have knowledge of the initial circadian phase of the person to be treated. This is best achieved by the previously described embodiment known as the Constant Routine. However, it would be acceptable in most cases to infer such phase based on comparisons made to the body of normative phase data such as is contained within this specification, or in the literature in general.

The optimal lighting schedule in order to effect amplitude reduction is one in which bright light (ca. 7,000-12,000 lux) of approximately six hours' duration is centered around the time of the endogenous temperature minimum as determined by the embodiment of the Constant Routine or normative data. A seven-to-eight-hour episode of absolute darkness (sleep) ideally should be placed in a position such that the midpoint of the dark episode is 180° (12 hours) from the mid-point of the bright light exposure. This regimen is repeated for two days in the preferred embodiment.

Slight modifications in the timing of the light or dark stimulus will result in a partial attenuation of amplitude, most likely with an attendant alteration in phase. If this schedule were substantially altered or inverted, one could expect an increase in circadian amplitude, if amplitude were initially at a nominal or sub-nominal value.

FIG. 31 illustrates the actual measured core body temperature of a human subject as a function of time. The subject underwent Constant Routines beginning at times indicates by 1402 and 1408. Between these two Constant Routines, however, two bright light episodes indicated as 1404 and 1406, were imposed.

An amplitude reduction to near zero is shown at 1410, after the commencement of the second Constant Routine. After time 1410, the peak-to-peak amplitude of the endogenous circadian pacemaker, as measured by the fitted core body temperature variation was reduced from 2°-3° F. to a level below detection.

As particular examples of lights used during experiments, during light exposure (7,000-12,000 lux, comparable in intensity to natural sunlight just after dawn), each subject was seated facing a bank of lamps and instructed to look directly at them for 5 minutes out of every 10. Reported light intensities are based on illuminance measurements recorded at 5-minute intervals from research photometers (International Light, Newburyport, Mass.) using a detector with a photopic spectral bias and a cosine angular response placed at the forehead and directed toward the line of gaze.

The bright light was provided by one of the following:

(1) A wall -mounted bank of 60-80 8-foot, 96-watt ion-gard F96TH12 Vitalite wide-spectrum fluorescent lamps (Duro-test Corp., North Bergen, N.J.), separated from the subject by floor-to-ceiling panels of either a 0.25 inch thick sheet of clear plexiglass or two 0.125 inch thick sheets of clear glass separated by a layer of polyvinylbutyl plastic (laminated safety glass);

(2) A bank of 60-80 8-foot, 60-watt F96T12/CW/EW cool-white econo-watt fluorescent lamps (North American Phillips Lighting Corp., Bloomfield, N.J.), separated from the subject by floor-to-ceiling panels as described above; or

(3) A portable bank of 16 4-foot, 40-watt lamps, either wide-spectrum vitalities or cool-whites, separated from the subject by a wire-mesh screen.

In our studies, the phase shifts induced by exposure to these different light sources have been equivalent for a given level of illuminance (as measured in lux or foot-candles), perhaps indicating the level of illuminance, as such, may be the critical factor affecting circadian phase shifting. Of course, the present invention contemplates that further optimizations of light protocols according to the present invention may include some emphasis on light of different regions in the spectrum. Indeed, the potential social obtrusiveness of certain bright lights may motivate research to conclude that only certain colors of light, or even light beyond the visible spectrum, may be effectively employed without drawing so much attention to the subject as bright white lights. Furthermore, ceiling mounted lights may be calibrated in brightness to consider the overall reflectance of walls, floors, ceilings, and other surfaces to deliver the proper intensity of light to the retina to accomplish the desired phase shifting or amplitude modification contemplated by the present invention.

In all three cases, the subjects' daily exposure to ultraviolet light during the trials was well within the safety guidelines for permissible ultraviolet light exposure established by the American Conference of Governmental Industrial Hygienists and the U.S. Army and recommended by NIOSH (Documentation of the Threshold Limit Values and Biological Exposure Indices, Fifth Edition (American Conference of Governmental Industrial Hygienists, Inc., Cincinnati, 1986); D. H. Sliney, Am J Optom Physiol Opt 60, 278 (1983); National Institute for Occupational Safety and Health, Criteria for a Recommended Standard, Occupational Exposure to Ultraviolet Radiation (National Technical Information Service, Rockville, Md., 1972, Government Publication Number PB-214 268)).

As an additional safety measure, all of our subjects now wear coated polycarbonate ultraviolet-excluding clear Ultra-spec 2000 safety glasses with 4C coating (Uvex Winter Optical, Inc., Smithfield, R.I.) throughout exposures to bright light. Given the negligible level of ultraviolet light to which our subjects are now exposed, we conclude that UV light exposure is not responsible for the phase resetting we have observed.

d. Increasing Circadian Amplitude Using Experimental Data

Increasing circadian amplitude is desirable in those individuals who are or wish to be stably entrained to a schedule to which they are already phase aligned. By increasing circadian amplitude, the circadian timing system is made more resistant to perturbations. Such an increase in amplitude may benefit a straight night shift worker who wishes to be entrained to the night schedule, yet on weekends tends to alter his schedule to facilitate his social life. Likewise, the straight day worker whose amplitude was increased could better tolerate a few late weekend nights and still be prepared for work early Monday morning. Thus, it is conceivable that augmented morning light exposure, either through appliances in the home or work place, or by way of a portable device on the way to work, will improve daily alertness, performance and memory, which are known to fluctuate with the core body temperature cycle. (See Czeisler, C. A., Kennedy, W. A., Allan, J. S., "Circadian Rhythms and Performance Decrements in the Transportation Industry." Proceedings of a Workshop on the Effects of Automation on Operator Performance, Coblenz, A. M., ed., Commission des Communautes Europeennes, Programme de Recherche Medicale et de Sante' Publique, Universite Rene Descartes: Paris, 1986, pp. 146-171.)

There is a range of amplitude augmentation which can be achieved using specifically timed regimens, which optimally include both periods of darkness and periods of bright light exposure. It is possible to effectively increase circadian amplitude in one or two days of scheduled light exposure.

In order to best design the lighting schedule, one must have knowledge of the initial circadian phase of the person to be treated. This is best achieved by the previously described embodiment known as the Constant Routine. However, it would be acceptable in most cases to infer such phase based on comparisons made to the body of normative phase data such as is contained within this specification or in the literature in general.

The optimal lighting schedule in order to effect amplitude augmentation is one in which bright light (ca. 7,000-12,000 lux) of approximately four to six hours' duration is diametrically opposed to the time of the endogenous temperature minimum as determined by the embodiment of the Constant Routine or normative data. A seven-to-eight-hour period of absolute darkness (sleep) ideally should be centered around the endogenous temperature minimum. Bright light exposure in the morning or evening can also enhance endogenous circadian amplitude. This regimen may be applied chronically, if desired, as the amplitude of the circadian timing system over several weeks' time will slowly return to a nominal value following an amplitude perturbation.

The left panel of FIG. 32 shows a pre-intervention Constant Routine assessment of the endogenous circadian temperature rhythm of a normal male subject. The right panel shows the result of the post-intervention phase and amplitude assessment following seven days of morning bright light exposure (4 hours per day). Note that there is little change in the phase of the endogenous temperature cycle minimum; however, there is a marked increase of the amplitude of the rhythm.

Slight modifications in the timing of the light or dark stimulus will result in a partial augmentation of amplitude, most likely with an attendant alteration in phase. If this schedule were substantially altered or inverted, one could expect a decrease in circadian amplitude, if amplitude were initially at a nominal or supra-nominal value.

5. Theoretical (Model-Based) Foundation for the Inventive Techniques to Modify Circadian Phase and Amplitude

The endogenous (deep) circadian pacemaker, hereafter designated as "the x oscillator," or simply "x," may be modelled mathematically by a second-order differential equation of the van der Pol type, specifically: ##EQU1##

In the absence of any forcing function, F_(x), x will have an approximately sinusoidal waveform with an amplitude of 1 (that is, the full excursion of x from a maximum of+1 to a minimum of -1 will be 2).

The forcing function, F_(x), consists of two effects. The dominant effect is that of the light to which the retina is exposed. The secondary effect is due to endogenous internal influences of the activity-rest pattern.

In the form given above, time t is measured in clock hours. The parameter m_(x) is the "stiffness" of the x oscillator and for normal humans is expected to be in the range 0.05≦m_(x) ≦0.15 with 0.1 as the representative value. The estimate of 0.1 for m_(x) was originally chosen as a trial value by analogy with the value of m_(y) (the internal "stiffness" of the y oscillator) of our dual oscillator model of the human circadian timing system which had been validated by earlier experimentation characterizing a phenomenon called phase trapping. Our experimental success in manipulating the amplitude of the oscillatory output implies that m_(x) is very unlikely to be larger than 0.15, and certainly not larger than 0.2. An oscillator with an internal stiffness coefficient less than 0.03 would be unreasonably susceptible to external influences and therefore physiologically incompatible with the observed robustness of the endogenous circadian ("x") oscillator sensitive in this context. The parameter T_(x) represents the intrinsic period of the x oscillator and for normal humans is expected to be in the range 23.6≦T_(x) ≦25.6 with 24.6 as the representative value.

For most people in the age range 5 to 55 years, sleep occurs in a single consolidated episode each 24 hour day. In the laboratory paradigm of "free run" (self-selected sleep and wake) the sleep/wake cycle time for young adults is typically in the 25 to 26h range. About 30% of free run experiments lead spontaneously to internal desynchrony in which the sleep/wake cycle time exceeds 30 hours (ranging up to 50 hrs) while the core body temperature rhythm proceeds at about 24.5h. We ascribe these separate rhythms to distinct rhythm generators: y for the labile sleep/wake process and x for the "deep circadian pacemaker". In synchronized free run the interactions between y and x produce mutual entrainment, and since the compromise cycle time, T, is biased strongly toward T_(x), it follows that the action of y on x is only about 25% of the action of x on y.

In our proposed dual oscillator model, (see R. E. Kronauer et al., "Mathematical Model of the Human Circadian System with Two Interacting Oscillators," Am. Journal of Physiology, Vol. 242, pp. R3-R17, 1982, hereby incorporated by reference) x and y are distinct van der Pol oscillators coupled via linear velocity-dependent terms. With a revised amplitude scaling the model is: ##EQU2##

Environmental influences readily affect the y process directly. Laboratory experiments in which light level was uniform throughout waking hours indicated unambiguously that imposed time shifts acted upon the x process thou h they came via y in this model structure.

There are two alternative explanations for this rent action. The first is that sleep and wake directly influence the x pacemaker (known to reside in the suprachiasmatic nuclei) thru internal mechanisms (e.g. hormones). The second follows from the turning off and on of ambient light in precise synchrony with the sleep/wake timing. If the cyclic modulation of light is influencing x, it would appear exactly like a direct y-to-x influence. A quantitative comparison of the ability of laboratory light cycles to entrain x with the inability of the sleep/wake cycle to entrain x in blind subjects tells us that room light represents over 70% of the entrainment effect in sighted persons and well over 90% when light is increased to a few thousand lux. Consequently, we will consider the effects of light on x first.

A standard measure of the illuminance of the scene on which a human observer gazes is the foot-candle or the lux. This measure differs from the total light power on the visible spectrum since it is weighted by photopic luminosity function. That is, those portions of the visible spectrum to which the visual system is more sensitive are more heavily weighted. In formula 2, below, I denotes the illuminance of the scene of gaze (averaged over all of the directions of gaze encompassed by the retina). B denotes the subjective brightness which an observer associates with I. Stevens, Science, Vol. 133, pp. 80-86 (1961), has shown that over a wide range of I (about 6 log units), B is related to I by:

    B=cI.sup.1/3                                               (2)

where c is constant to be determined. The forcing function due to light actions on the retina is taken to be ##EQU3## This representation is a novel embodiment of three hypotheses: (1) subjectively assessed brightness is the appropriate measure of the effect of light on the circadian pacemaker, (2) the x oscillator responds predominantly to changes of brightness and not, significantly, to sustained or average brightness, and (3) the brightness coefficient, c, may depend on the time (i.e, phase) of the circadian cycle at which it is measured (and consequently c has been placed inside the time-derivative operator).

The exponent, 1/3,is substantially valid over a wide range of I. It is to be understood that exponents in a range about 1/3 (such as 1/6-1/2) are within the contemplation of the present invention, as are differing exponents for different ranges of I (for example in extremely bright or extremely dim environments).

The coefficient c which is appropriate for normal human subject during ordinary waking hours and when I is measured in lux is in the range 0.05≦c≦0.1 with c=0.069, for instance, as a representative value. The value for c is chosen on the basis of laboratory experiments conducted in ordinary room light in which entrainment occurred to an imposed period differing from T_(x) by ±1.0-1.3 hours (and the exposure to this light occurred principally during ordinary waking phases of the x cycle) ; and on the basis of the observation that blind subjects cannot entrain to periods which differ from T_(x) by 0.4 hours. If the time history of light (including darkness, which is the absence of light) to which the retina is exposed is specified in lux, as I(t), then application of equation (3) gives the light-component of the forcing function, F_(x), suitable for use in equation

Since brightness is the surrogate for y in the second explanation for the action of on x, we rewrite (1A) as: ##EQU4##

Measurements of electical activity in the retina induced by light (electroretinogram, ERG) show circadian variations, particularly in the "B wave". Psychophysical data show comparable variations in perceptual sensitivity, with sensitivity being twice as high at 0400 as at 1600. The data of R. Knoerchen and G. Hildebrandt, J. Interdisc Cycle Res 7, 51 (1976) on the absolute sensitivity of the human visual system show that the sensitivity is about twice as high when x is at its minimum (approximately 3 AM to 4 AM in normally entrained young adults) than when x is at its maximum (3 PM to 4 PM). This result applies equally to cone-mediated sensitivity and rod-mediated sensitivity and consequently suggests a post-receptor variation in system sensitivity.

We have reported enhanced sensitivity of the human circadian pacemaker to bright light applied at night. The effect of circadian modulation of this sensitivity to light is most simply accomplished by redefining brightness:

    B=(1-mx)CI.sup.1/3                                         (2A)

where m is a "modulation index (m=1/3 corresponds to perceptual data).

The second order differential equation (4) requires a 2-dimensional phase space for its representation. Mathematically, a second order equation can always be converted to a pair of coupled first order equations. The latter form is more general; reflected in the fact that the tranformation of (4) to a first order set is not unique. We choose a transformation proposed by Lienard: ##EQU5##

This transformation is not simply cosmetic. Rather it conveys several fundamental truths. One truth is that the basic variable, x, has an associated "complementary" variable, x_(c), which has an equal claim to "basicness". A second truth is that the differentiation of B which appears in eq. (1C) gives a misleading idea that only changes of brightness affect the x oscillator. In fact eq. (1D) shows that B (not its time derivative) affects the derivative of x and that changes in x are due to an integration of B over time. Simply stated, the effects of B on x are cumulative in this model.

Altered Amplitude

The amplitude of the x rhythm is conveniently defined as:

    A.sub.x =(x.sup.2 +x.sub.c.sup.2).sup.1/2

Light can alter the amplitude as well as the phase of x. For example, when light is applied to x near its minimum (which corresponds to the phase of endogeneous temperature minimum, or about 0400 under ordinary conditions) the resulting increase in x acts to decrease |x| and hence to decrease A_(x). Although the van der Pol oscillator proceeds to restore its amplitude back toward the reference value A_(x) =1, the restoration takes time (several daily cycles) to be complete.

Through stimulus repetition on successive days the cumulative change in A_(x) can be made large enough to reduce A_(x) essentially to zero. This is the fundamental process underlying "type 0" resetting which we have demonstrated with 3 successive exposures to 5h episodes of 10,000 lux.

Although "type 0" resetting necessarily implies the ability to drive an oscillator to (and through) the zero-amplitude condition we have undertaken to demonstrate the attainment of zero amplitude experimentally. Two exposures of 10,000 lux for 5.5h on successive days have proven to be a stimulus of correct strength, but the timing of this stimulus has proven to be extremely critical. Nevertheless we have been able to reduce the amplitude of the endogenous temperature rhythm in 2 subjects to less than 16% of their ordinary amplitude, and in another 6 subjects to less than 32%.

The second effect of light

By exposing subjects, whose amplitude has been greatly reduced, to additional single 6h episodes of 10,000 lux we have discovered, and have come to understand in model terms, the basis for the criticality of stimulus timing (i.e. the property of x which is responsible for the difficulty in reducing amplitude very close to zero). Simply stated, the complementary variable x_(c), also responds to light; something which we had not anticipated. This action of light is to "repel" x_(c) away from x_(c) =0. The effect can be incorporated int eq. (1E) thus: ##EQU6##

As eq. (1F) shows, this additional effect is remarkably strong since brightness enters eq. (1F) with the same strength which it exerts in eq. (1D)

Equations (1D) and (1F) are now the constitutive equations for the deep circadian pacemaker. They describe both the intrinsic self-sustaining properties of the van der Pol system and the forcing effects of light (whatever the amplitude and phase of x at which light is applied). To understand how light works, it is convenient to consider a brief, strong episode; in particular, 2h of 10,000 lux.

For short times the equations (1D) and (1F) can be integrated by holding the variables on the right side constant during the integration. The changes produced by light can be sorted out separately: ##EQU7##

where x and x_(c) values correspond to the center of the brief episode. The parameter values are: ##EQU8##

FIG. 41 shows Dx and Dx_(c) (in vector form) for a variety of reference (x,x_(c)) points (i.e., x and x_(c) corresponding to the midpoint of bright episodes). For convenience the nominal A_(x) =1 circle is indicated and clock hours corresponding to the normal person's entrained state have been shown.

The divergence of the vector field away from x_(c) =0 shows graphically how difficult it is to drive x to the zero-amplitude "target" (x=0,x_(c) =0) . We see al so that light acts generally to enhance amplitude. The ability of light to shift phase of x is almost nil for clock hours from about 1200 to 2000. Bright episodes are most effective in shifting phase forward at about 0800 and backward at about 2400.

As metioned above, the data of R. Knoerchen and G. Hildebrandt, J. Interdisc Cycle Res 7, 51 (1976) on the absolute sensitivity of the human visual system show that the sensitivity is about twice as high when x is at its minimum (approximately 3 AM to 4 AM in normally entrained young adults) than when x is at its maximum (3 PM to 4 PM). This result applies equally to cone-mediated sensitivity and rod-mediated sensitivity and consequently suggests a post-receptor variation in system sensitivity. The measured circadian sensitivity variation can be represented approximately by a cosine function. Since x is also a cosine function c may be adequately represented by

    c=a-bx

where the data of Knoerchen and Hildebrandt imply b=a/3. Our fitting of human phase response data gives a preliminary estimate of b=2a/3. There is no physiological requirement that these two sensitivity variations be exactly the same since they have different neural pathways. The circadian data, as further refined, are the definitive ones. We interpret a to correspond to the value of c deduced above from entrainment limit experiments (for instance, a=0.065).

The endogenous, non-light forcing function onto the x oscillator is included in the model by an activity function G(t) which takes on the value 0 during sleep and a constant value G_(o) during wakefulness. The activity forcing function is: ##EQU9## Since G(t) takes on only two values, 0 or G_(o), and the transitions between them take place relatively abruptly in time, the time derivative is singular at each transition and is represented mathematically as a "d-function." When the transition is from sleep to wakefulness, the d-function has the strength G_(o) ; when the transition is from wakefulness to sleep the d-function has the strength -G_(o). For normal human subjects 0.03≦G_(o) ≦1.15 with G_(o) =0.06 as the representative value which is compatible with the entrainment data of blind subjects. In circumstances where sleep is associated with dark episodes, it is possible to infer G(t) from the temporal pattern of light and dark and so its effect on x becomes mingled with direct effects of light on x. Totally blind subjects display clearly the effects of G(t), since the direct effect of light is absent. Since in normal, sighted persons the effect of A is much smaller than ordinary environmental light effects, it is difficult to estimate this effect accurately.

With the descriptions given, a complete solution for x(t) can be generated computationally by an integration procedure such as the Runge-Kutta method from equation 1 if, at some initializing time, values for x and dx/dt are assigned and the subsequent temporal patterns of G(t) and B(t) are specified. The forcing function F_(x) is represented as the sum of the two components: ##EQU10## Assuming that the light is within normal environmental ranges and that sleep episodes are regularly used, as time proceeds, the solution X(t) will depend progressively less and less on the specific initial conditions assigned.

Mathematical Representation of Human Circadian Phase Resetting Data

To summarize data found in studies of the effects of light on circadian rhythms, a mathematical representation characterized by relatively few parameters approximates our understanding of essential circadian pacemaker properties. Based on a demonstration of a direct action of light on that pacemaker, the preferred mathematical model for the effect of light on the human circadian pacemaker may be represented as a van der Pol oscillator.

When stimuli are extended in time, the intrinsic tendency of such a van der Pol oscillator to revert it to its nominal amplitude would ordinarily act cumulatively to oppose stimulus-induced changes. However, if the oscillator's resiliency is weak (i.e., its "stiffness" is low), then even an extended time stimulus can be approximated as an equivalent impulsive stimulus.

Under such conditions (a low stiffness oscillator), the asymptotic form achieved by this model (in the limit of weak stiffness) can be represented as: ##EQU11## where small deviations of intrinsic circadian period from 24 hours are accommodated by the phase shifts, a and φ_(c), and the parameter b represents a modulation of the effectiveness of light depending on the circadian phase of its application.

Using non-linear least squares, the mathematical representation in the mathematical model according to the preferred embodiment of the present invention was fit to the data in FIG. 15B, Panel C, and then was projected onto FIGS. 15B, Panels A and B. As shown by the solid line in FIG. 15B, the data are well described by this four-parameter representation. The standard error of φ_(f) in the preferred model, based on these particular results, is 1.99 hours, which is comparable to the observed error in a similar model of phase resetting to light in Drosophila pseudoobscure. The squared multiple correlation coefficient R² is 0.88 for data as plotted on the phase response curve of FIG. 15B, panel A. and is 0.73 for the data plotted on the phase resetting curve in panel C of FIG. 15B (where the ordinate is restricted to a narrower range).

These findings are consistent with similar mathematical representations of circadian phase resetting in which the light stimulus acts on the oscillator, altering both its phase and amplitude and consequently producing Type 0 as well as Type 1 resetting (depending on stimulus strength). However, based on data from both animal and human studies, the preferred model includes parameters to account for the possibility that the effectiveness of the light stimulus may be modulated as the cosine of circadian phase, due in part to circadian variations in retinal/visual sensitivity. The preferred model thus incorporates not only the circadian phase, but also the level of retinal/visual sensitivity.

Endogenous circadian rhythms have been reported in diverse functions of the visual system in a wide array of species, including human visual sensitivity (R. Knoerchen and G. Hildebrandt, J interdisc Cycle res 7, 51 (1976)). While considerable evidence indicates that in some species the eyes contain a circadian oscillator (G. D. Block and S. F. Wallace, Science 217, 155 (1982); T. L. Page, Science 216, 73 (1982); M. Terman and J. Terman, Ann NY Aca Sci 453, 147 (1985)), an optic nerve transection study in mammals suggests that that oscillator is synchronized to the light-dark cycle via its neural connections to the central nervous system, not by the direct exposure of the eye to light (P. S. Teirstein, A. I Goldman and P. J. O'Brien, Invest Opthalmol Vis Sci 19, 1268 (1980)).

In the preferred model, the sum, (a+b), represents the sensitivity to the stimulus when applied at φ_(i) =0(i.e., at ECP_(min)), while (a-b) represents the sensitivity to the stimulus when applied at φ_(i) =12. Therefore, the ratio (a-b)/(a+b)=0.22 derived from the parameter estimation (given with respect to panel C) implies a substantial reduction of circadian sensitivity to light at φ_(i) =12 hours (relative clock hour 17:00). More data would be desirable in the band 9<φ_(i) <21 to estimate this ratio precisely. These data are consistent with reported circadian variations in visual sensitivity which, some have argued, may be driven by an oscillator in the eye itself.

6. Phase and Amplitude Modification Using Theoretical (Model-Based) Foundations a. Application of the Model to a Single Bright or Dark Episode

The objective in the application explained here is to make a quantitative assessment of the effects on the endogenous circadian (x) oscillator of a specific intervention in which the light level is altered. For example, what would be the effect on a passenger during a flight of six hours' duration in which the average cabin illumination was maintained at 10,000 lux rather than the customary low level which is assumed to be 30 lux? According to equation (2), taking C to have a representative value of 0.065 we find the two B levels to be

    bright: B=0.065 * (10,000).sup.1/3 =1.40

    low: B=0.065 * (30).sup.1/3 =0.20

Thus, for the six-hour flight B is increased by an amount delta B=1.20. Since B is assumed to be essentially constant for the six hours, db/dt is zero except at the beginning and end of the flight. At the beginning db/dt has a d-function of strength delta B and at the end db/dt has a d-function of strength -delta B. All other aspects of the subject's light and dark temporal pattern are presumed to be unchanged. The response of the differential equation (1) to a d-function of strength delta B is to have an abrupt increase of ##EQU12## by an amount ##EQU13## Let t₁ be the time in clock hours after the minimum of x at which the d-function of strength delta B is applied, then 15t₁ is the phase angle in degrees (after the minimum of x) at which it is applied. The abrupt increase in dx/dt will produce an abrupt change in the phase of x by an advance shift of ##EQU14## radians, assuming that the x oscillator is at its reference amplitude of unity. It will also produce a change of amplitude of amount ##EQU15## These are the phase and amplitude responses to elementary impulsive stimuli (abrupt change of light). If the negative d-function is applied at time t₂ (after the minimum of x), it will produce an advance phase shift of ##EQU16## radians and an amplitude change of ##EQU17## The entire bright episode provides a change which is the sum of these two: ##EQU18## Trigonometric identities permit them to be rewritten ##EQU19## These are the phase and amplitude responses for a bright episode of duration t₂ -t₁ centered at a time (t₁ +t₂)/2.

For the specific example of the six-hour plane flight, since t₂ -t₁ =6 h, sin 15 (t₂ -t₁)/2 sin 45°=0.707, it follows that ##EQU20## Suppose that this light episode i s given to a person on an eastbound flight which leaves California at 0900 and arrives in New York at 1500 (California time). If the person is a typical young male adult with the minimum of x (as displayed by endogenous core body temperature) at 0600 California time, then t₁ =3h and t₂ =9h so 15(t₁ +t₂)/2=90° and the phase advance is seen to be 1.7h. Thus, this acute light treatment will provide about 60% of the required phase advance from California to New York.

Suppose next that this exposure is given to a person flying westward from New York, departing New York at 1800 and arriving in California at 2400 (New York time). If this person's minimum of x is at 0600 (New York time), the typical value, then t₁ =12 and t₂ =18 so 15(t₁ +t₂)/2=225° and the phase shift is seen to be -1.2h (actually a phase delay of 1.2h), which is 40% of the delay required for the New York to California trip. Both of these examples involve the increase of brightness during the episode. The formulae (7) can be applied equally well to situations where light is reduced, simply by allowing the change delta B to be negative. Thus, suppose that a subject is shielded from light (of say, 10,000 lux) to which he/she is ordinarily exposed and kept in a totally darkened room for 4h: ##EQU21## Then delta B=-1.40. Since t₂ -t₁ =4h, sin(15(t₂ -t₁)/2=0.5 and

    Phase shift=-1.40 (π/6) (0.5) sin (15(t.sub.1 +t.sub.2)/2) (radians)

If, as assumed before, the minimum of x is at 0600 and the dark episode is centered about 1200, 15(t₁ +t₂)/2=90° and we have ##EQU22##

In summary, formulae (7) permit the calculation of phase and amplitude effects of any specific brightness intervention which is essentially constant over the duration of the intervention episode. It is necessary to specify both the imposed brightness and the brightness which it replaces in order to calculate the effects.

b. Application of the model to extended multiple exposure light and dark protocols

As the previous examples show, single episodes of reasonable brightness change lasting for reasonable durations can produce significant phase and amplitude changes, but less than are required for many common applications (for example, a 6h phase advance from N.Y. to Paris, or an 8h phase advance for a change of working shift). There is, therefore, a need for stronger effects and a need to program light and dark temporal patterns for extended time. To reduce somewhat the multitude of options, we will present the analysis for protocols which are cyclic with a 24h cycle time. That is, we will consider the effects of light/dark temporal patterns which are specified for 0≦t≦24 and repeated on a 24h basis some integral number of times.

It was discovered that the strength of the phase-shifting drive is roughly proportional to the cube root of the illuminance, in lux. Thus, the earlier assumption by Lewy et al.--that any light of less than a 500-lux threshold could be equated with darkness for purposes of circadian analysis--appears to be incorrect.

This incorrect assumption was apparently related to a long-existing misconception that light was not a strong zeitgeber for the human circadian cycle. The effects of light much greater than 2,500 lux was not isolated in previous experiments which did not completely eliminate self-chosen light (100-300 lux) during periods of supposed "darkness" in the experimental procedures. The effect of applications of bright light was also masked by factors such as physical activity, posture, and timing of sleep episodes and feeding, in addition to the confounding influence of supposed "darkness" which was in fact not "dark", biologically.

It has been further discovered that it is not the bright lights, per se, that effectuate a phase modification. Rather, it is changes in light intensity that cause phase modifications. Although a 15-minute period of half illumination was used before and after "pulses" of bright light to acclimatize the subjects, it has been found that it is the change in light intensity, and not the bright light itself, which is the most direct causal factor in circadian phase shift. (In this discussion, the term "pulse" is not limited to a pulse of short duration; in fact, the duration of light pulses in the preferred embodiments of the present invention are on the order of three-six hours long. Conversely, Pittendrigh determined that pulses with durations on the order of milliseconds had profound effects on fruit flies living in otherwise total darkness.)

The first important observation is that an oscillator with low stiffness, such as m_(x) =0.1, is a very effective band-pass filter. This means that it responds predominantly to excitation at or near its resonance period, T_(x). This means that for forcing patterns which have a 24h cycle it is the fundamental Fourier component (i.e., the component in the Fourier series expansion of the forcing pattern with a period of 24h) which is principally responsible for secular (i.e., time-cumulative) shifts of phase and amplitude of x oscillation. Thus, different forcing patterns which have the same Fourier fundamental will have approximately the same cumulative effects on phase and amplitude. Different effects may be encountered for two forcing patterns with the same Fourier fundamental when the cumulative effectives per cycle are large (e.g., amplitude changes in excess of 0.6 or phase shifts in excess of 3h per cycle).

To systematize the presentation and summary of the effects of cyclic protocols we introduce the concept of the "cyclic stimulus vector," or simply "stimulus vector." The magnitude of this vector is π² /12 times the magnitude of the Fourier fundamental of the brightness pattern, B(t). The phase (or time of action) of this vector is the time at which the Fourier fundamental achieves its positive maximum value within the 24h cyclic stimulus which we denote t_(m). Then, if the cyclic pattern is initiated at some phase after the minimum of x, which we denote t_(p), the phase of the stimulus vector after the minimum of x, t_(s), is:

    t.sub.s =t.sub.m +t.sub.p

Thus, the effects of cyclic stimuli found by computational simulations will be classified according to

(1) The magnitude of the stimulus vector;

(2) The phase of the stimulus vector, t_(s), for the first cycle of stimulus application; and

(3) The number of stimulus cycles, N.

These ideas are embodied in the example shown in FIGS. 33A, 33B 33C, 34 and 35.

In FIGS. 33A, 33B, 33C a stimulus cycle is shown which contains both a dark episode of 8h duration and a bright light episode (9,500 lux) of 5.5h duration. Otherwise the brightness is equivalent to 175 ; lux of laboratory light. It is assumed that darkness corresponds to sleep and any light represents wakefulness so G(t) is known. The total stimulus is G(t)+B(t). Also in FIG. 33C the Fourier fundamental is shown and the corresponding stimulus vector, defined above. It is seen that t_(m) =12h and the stimulus vector magnitude is 0.55. Computer simulations have been performed using the representative period, T_(x) =24.6h, and locating the stimulus vector at various t_(s). The standard amplitude of unity has been used as the initial value for x and the solutions have been started at the end of the dark episode. At the ends of succeeding dark episodes, N times 24h later, the amplitudes and phases of the computed x are measured.

The changes of phase from the initial x phase (in hours) are reported on the phase shift diagram of FIG. 34 for N=1, 2, 3, and 5. These are analogs of "phase response curves" (PRC) reported for other species, but whereas the conventional PRC are for briefly applied light stimuli, those of FIG. 34 are for extended light/dark protocols. We observe that N=1 gives a PRC which is known as "Type 1 resetting" while N=3 and 5 give "Type 0 resetting." N=2 is very close to the borderline between these types but is in fact "Type 1".

FIG. 35 shows the amplitudes produced by the various N cycles and depicts amplitude response curves (ARC). It can be seen that the critical nature of N=2 (borderline between "Type 1" and "Type 0") is due to the reduction of amplitude virtually to zero. FIG. 34 shows that one cycle of this stimulus strength can produce at best 2h of phase advance or 3h of phase delay. (The asymmetry reflects the fact that x has a period, T_(x), which is 0./6h longer than the 24h protocol . Similarly, 2 cycles can produce at best 4.2h advance or 6.2h delay (or 2.1h and 3.1h per cycle, respectively). In contrast, 3 stimulus cycles can produce any desired phase shift (up to 12h advance or 12h delay) because of the great reduction in the amplitude of the x oscillation on the intermediate cycles. Furthermore, after the full 3 stimulus cycles the amplitude is greatly restored, never being less than 60% of the original value and in many conditions being more than 35% larger than the original value.

The experimental data derived from laboratory studies have been organized according to the phase of the cyclic stimulus vector being applied, as described just above, developed as part of this invention. As can be seen in FIG. 36, the comparison between the experimentally derived data and the model computations is quantitatively satisfactory. Furthermore, when organized in this manner, the experimental data themselves become internally consistent, thereby resolving the ambiguity and multivaluedness of the data as presented either in the classical phase response curve (PRC) to light, organized by the circadian phase of light administration, shown in FIG. 11 or in the newly recognized organization of the data based on the phase of dark episode timing, as in FIG. 14. Neither the representation of FIG. 11 nor that of FIG. 14 simultaneously take into account the phase of both light exposure time and dark exposure time, which is accomplished in the cyclic stimulus vector diagram of FIG. 36.

C. Stopping the x Oscillation

From the ARC (Amplitude Response Curve) of FIG. 35 we find that two cycles of a strong cyclic stimulus can reduce the amplitude of the x oscillation to extremely low values. At an amplitude of zero the circadian clock can be said to have been "stopped."

To be of use in studies of the effects of this unusual condition it is necessary to bring a subject precisely to this state under appropriate laboratory or environmental conditions. Typically this means that zero amplitude should be achieved upon a wake-up into the desired environment. If we suppose that we have some approximation to a protocol which might bring a subject from an experimentally-determined initial state (the amplitude and reference phase of x having been deduced from the core body temperature of a Constant Routine, for example) it is not a straightforward or simple matter to modify the protocol to suit a specific subject. The difficulty is that the zero-amplitude or "stopped clock" condition is, mathematically speaking, a "small target" and for the differential equation (1) which describes the x oscillator and the natural tendency of solutions is to move away from that condition. (That is, the zero-amplitude condition is an unstable singular point.)

Consequently the protocol must be "fine-tuned" to the specific subject and his/her initial state. Ideally the subject's intrinsic period, T_(x), should first have been measured experimentally (as, for example, through internal desynchrony forced by placing the subject on a sleep/wake cycle of 28h period). Then the differential equation, together with the candidate approximate protocol, should be integrated backwards in time, beginning at zero amplitude (which is the desired end state). If the candidate protocol does in fact have a usable solution, the solution for x will have an amplitude which grows (backwards in time) until it passes through the amplitude which has been ascribed to the subject's initial state. The point in this reversed-time solution which exactly matches the subject's amplitude is now the onset point for the protocol and the timing of all events in the protocol is given by returning to "forward time." Furthermore, the phase of x at this precise solution point establishes the relationship between the time at which the protocol commences and the time of the minimum of x.

Clearly there are many clock-stopping protocols which can be developed using this model. Cyclic protocols are usually required and those which involve a strong stimulus vector will achieve zero-amplitude in fewer clock hours. This is especially desirable if the subject's T_(x) is not accurately known (as, for example, it is estimated on the basis of normative data relating to the subject's age and sex), since errors in T_(x) produce cumulative phase errors during any protocol in direct proportion to protocol duration. Protocols which attain the initializing amplitude during a sleep episode may have to be rejected if the fraction of the sleep episode which remains within the protocol is judged to be too short to serve the appropriate sleep function. This condition can generally be eliminated by altering the strength of the stimulus vector (by changing the duration of bright episodes, for example).

What follows is a description of a particular protocol for manipulation of the amplitude of the endogenous (deep) circadian pacemaker.

FIGS. 37 and 38 illustrate a phase plane diagram and a timing diagram, respectively, of the phase and idealized core body temperature of a subject whose deep circadian pacemaker amplitude is being reduced to near zero.

This idealized experiment begins with the endogenous circadian pacemaker at a minimum at 1202/1302. Between times 1204/1304 and 1206/1306, the subject rested or slept, in darkness. After a period of ordinary diurnal activity, the subject was then exposed to bright light from time 1208/1308 until 1210/1310. As indicated at 1210, the bright light episode has substantially reduced the amplitude of the endogenous circadian pacemaker.

A succession of diurnal activity, bedrest, diurnal activity, and another bright light episode is repeated at times delimited by 1212/1312, 1214/1314, 1216/1316, and 1218/1318. A significant reduction in amplitude of the endogenous circadian pacemaker is indicated at 1218. After one more period of diurnal activity and another episode of bedrest in darkness, the subject entered a Constant Routine for 24 hours. By this time, the amplitude of the endogenous circadian pacemaker had been reduced by the previous bright light episodes. The amplitude of the endogenous circadian pacemaker has effectively been reduced to zero.

The application of a bright light pulse at any point after the amplitude is zero results in the instant resetting of the deep circadian pacemaker to a newly defined phase. The virtual instantaneousness of this phase resetting represents the extreme demonstrated by the difference of the phase traversals already indicated in FIG. 37. Specifically, it is evident that the phase shift during the second bright light episode 1216 to 1218 is greater than the phase shift during the first bright light episode 1208 to 1210. This enhancement of the phase shift is based on a reduction in the endogenous circadian pacemaker amplitude. When the amplitude is reduced in the extreme, that is, to an amplitude zero, any desired phase shift may be achieved in a diminishingly small period of time.

By increasing the time of exposure to the bright light and scheduled darkness, the time required to reduce the circadian amplitude to zero is minimized. FIG. 38A illustrated a timing diagram in which the circadian amplitude is reduced to near zero in less than 1.5 days.

In FIG. 38A, the three 8.5 hour controlled darkness bed rest periods from FIG. 38 have been replaced by two controlled darkness bed rest periods which have extended in duration to about 8-12 hours; the two 5.5 hour bright light periods have been replaced by a single bright light period which has been extended in duration to about 8 hours. Considerations of practicality may require shorter periods of exposure or alterations of timing of the periods, but the effect of such variations may readily be predicted by application of the principles of the invention (through use of the preferred mathematical model or otherwise) to individually measured circadian data (using, for example, the Constant Routine), or to empirically derived normative data.

Thus, the invention contemplates a method of reducing the circadian amplitude of a subject to a small amplitude approaching zero in less than 1.5 days, comprising the steps of exposing the subject to darkness during a first period of approximately 8-12 hours, the first time period being roughly centered on a predicted amplitude maximum of the endogenous circadian pacemaker; exposing the subject to bright light during a second time period, the second time period being roughly centered on a predicted amplitude minimum of the endogenous circadian pacemaker; and exposing the subject to darkness during a third period of approximately 8-12 hours, the third time period being roughly centered on a predicted amplitude maximum of the endogenous circadian pacemaker.

The invention also contemplates following the above method with a light stimulus which immediately resets the circadian phase to a desired phase.

FIG. 31 illustrates the actual measured core body temperature of a human subject as a function of time in an actual experiment utilizing the principles of the present invention. The subject underwent Constant Routines beginning at times indicated by 1402 and 1408. Between these two Constant Routines, however, two bright light episodes, indicated as 1404 and 1406, were imposed.

An amplitude reduction to near zero is shown at 1410, after the commencement of the second Constant Routine. After time 1410, the peak-to-peak amplitude of the endogenous circadian pacemaker, as measured by the fitted core body temperature variation, was reduced from 2°-3° F. to a level below detection.

As particular examples of lights used during experiments, during light exposure (7,000-12,000 lux, comparable in intensity to natural sunlight just after dawn), each subject was seated facing a bank of lamps and instructed to look directly at them for 5 minutes out of every 10. Reported light intensities are based on illuminance measurements recorded at 5-minute intervals from research photometers (International Light, Newburyport, Mass.) using a detector with a photopic spectral bias and a cosine angular response placed at the forehead and directed toward the line of gaze.

The bright light was provided by one of the following:

(1) A wall-mounted bank of 60-80 8-foot, 96-watt ion-gard F96TH12 Vitalite wide-spectrum fluorescent lamps (Duro-test Corp., North Bergen, N.J.), separated from the subject by floor-to-ceiling panels of either a 0.25 inch thick sheet of clear plexiglass or two 0.125 inch thick sheets of clear glass separated by a layer of polyvinylbutyl plastic (laminated safety glass);

(2) A bank of 60-80 8-foot, 60-watt F96T12/CW/EW cool-white econo-watt fluorescent lamps (North American Phillips Lighting Corp., Bloomfield, N.J.), separated from the subject by floor-to-ceiling panels as described above; or

(3) A portable bank of 16 4-foot, 40-watt lamps, either wide-spectrum vitalities or cool-whites, separated from the subject by a wire-mesh screen.

In our studies, the phase shifts induced by exposure to these different light sources have been equivalent for a given level of illuminance (as measured in lux or foot-candles), perhaps indicating the level of illuminance, as such, may be the critical factor affecting circadian phase shifting. Of course, the present invention contemplates that further optimizations of light protocols according to the present invention may include some emphasis on light of different regions in the spectrum. Indeed, the potential social obtrusiveness of certain bright lights may motivate research to conclude that only certain colors of light, or even light beyond the visible spectrum, may be effectively employed without drawing so much attention to the subject as bright white lights. Furthermore, ceiling mounted lights may be calibrated in brightness to consider the overall reflectance of walls, floors, ceilings, and other surfaces to deliver the proper intensity of light to the retina to accomplish the desired phase shifting or amplitude modification contemplated by the present invention.

In all three cases, the subjects' daily exposure to ultraviolet light during the trials was well within the safety guidelines for permissible ultraviolet light exposure established by the American Conference of Governmental Industrial Hygienists and the U.S. Army and recommended by NIOSH (Documentation of the Threshold Limit Values and Biological Exposure Indices, Fifth Edition (American Conference of Governmental Industrial Hygienists, Inc., Cincinnati, 1986); D. H. Sliney, Am J Optom Physiol Opt 60, 278 (1983); National Institute for Occupational Safety and Health, Criteria for a Recommended Standard, Occupational Exposure to Ultraviolet Radiation (National Technical Information Service, Rockville, Md., 1972, Government Publication Number PB-214 268)).

As an additional safety measure, all of our subjects now wear coated polycarbonate ultraviolet-excluding clear Ultra-spec 2000 safety glasses with 4C coating (Uvex Winter Optical, Inc., Smithfield, R.I.) throughout exposures to bright light. Given the negligible level of ultraviolet light to which our subjects are now exposed, we conclude that UV light exposure is not responsible for the phase resetting we have observed.

7. Devices for Facilitating the Method a. Devices for the Administration of Light

Use of the methods of the invention requires that a person or group of persons may be exposed to light of the necessary intensity at the necessary time(s). The invention envisions many methods for illuminating an environment which can be adapted to this purpose. In particular, electric lights of either incandescent or fluorescent type can produce light of sufficient intensity when large numbers of them are concentrated on a surface. A wall eight feet high and ten feet wide covered with conventional fluorescent lamps spaced two to three inches apart (3800-5800 watts total) will create illumination sufficient to expose a person to 9,500 lux, measures of the pupil of the subject, at a distance of ten feet or so if the person's gaze is directed at the wall. Fluorescent lamps have the advantage that they emit light over their entire surface rather than at a single bright spot. Thus the light is diffuse enough that a person can stare directly at the glowing lamp from any distance without discomfort (although a person coming directly from a dark environment would require a adjustment period of partial illumination to allow the eyes to adjust). A similar wall bearing an array of incandescent lamps is also effective, but the intensity of light at the lamps' filaments may make it necessary to place a diffuser between the lamps and the viewer. The diffuser must be of heat-resistant material and the brightness of the lamps must be increased to compensate for the overall intensity and spectral loss of light caused by the diffuser.

If the lights are placed on the ceiling or an overhead flat surface, then the illumination of the user's eye is by light reflected from the surroundings rather than by light directly from the lamp (unless the user is in a supine or reclining position looking upward, in which case the situation is the same as with the lights mounted on a wall). Thus, the light must be brighter at the source to compensate for its absorption by surfaces and objects in the environment. However, since the user would not be gazing directly at the overhead light, sources with greater intensity can be used, such as high-intensity incandescent lamps, halogen lamps, arc lamps, mercury or sodium vapor lamps, or the sun. Use of natural sunlight via skylights or outdoor atria is precluded in most but not all cases because it is available only at certain hours and is subject to variation caused by season and weather.

Large banks of lights require large amounts of space and consume a great deal of energy. The cost of the space and the light fixtures may be too high for most individual users but can be offset if multiple users are expected, for example, in a public facility, factory or airplane. The energy used to power the lights--which is ultimately converted into heat--may be recycled by circulating the air heated by the fixtures and in the illuminated area and using it for heating purposes elsewhere. Many such installations would operate primarily in the winter when short daylight hours and cold outdoor temperatures limit the availability of sunlight, so the heat produced is of value. Ideally, the parts of the light installation creating the most waste heat such as the lamps, ballasts, and dimmers, are enclosed and ventilated separately from the surrounding area; the heated air exhausted from the enclosure is handled by ducts and blowers incorporated into the environmental conditioning system of the building.

An alternative to large light banks are smaller lights placed closer to the user (FIGS. 39A, 39B, 39C) A bank of ten four-foot fluorescent lamps covering a three-foot by four-foot area and positioned vertically produces illumination of 9,500 lux at a distance of about 3 feet from the eye, if the user's gaze is toward the lamps. Halving the distance between the lights and the user allows halving each dimension of the array and quartering the total light output while producing the same amount of light incident to the user's eye. Thus, a light fixture two feet wide and eighteen inches high suffices if it remains approximately eighteen inches from the user's face. Such a fixture is easily portable and can be mounted on a flexible positioning stand that would allow the user to place it at the ideal height, tilt, and distance. Such a fixture makes an ideal device for persons who must use the lights chronically. It may also be desirable to have such a device for home use. For example, morning exposure to bright light could both greatly improve daytime job performance and enhance nighttime sleep by amplifying circadian amplitude, which reinforces stable entrainment. This could be accomplished by incorporating lights into the headboard or above the headboard of the bed, in the bathroom or shower area, or by making the breakfast area into a solarium, using either natural or artificial lighting to achieve the desired intensity. The limitations in the user's movements caused by the closeness of the lights, and the boredom of having to gaze in a single direction, can be offset by leaving the spaces between the lamps open, thus permitting the user to focus his or her eyes on a television (or the like) placed a distance behind the fixture.

Another possibility is the use of localized retinal illumination through illuminated goggles (FIGS. 40A, 40B). The goggles provide a bright field of light, produced by small lamps within the goggles themselves, leaving a slit or other opening in the center through which the wearer can see. The light thus provided is fully portable, requires very little energy, and is easily controlled. The physical position of the goggles determines the precise distance from the lights to the eyes, making control of the illumination level very precise. Variations in light from the environment entering the openings can be compensated for by an electronic device incorporating a photodiode or phototransistor that senses the ambient light level and dims or brightens the goggles' internal lights accordingly.

While the use of localized retinal illumination through light-controlled goggles is appealing from the standpoints of portability, low energy requirement, precise timing, uniform controllability, and the mobility they afford the wearer, there are several considerations to be addressed. First, light scattering in the vitreous humor (due to the Tyndall effect) will add light to the fovea and parafovea, which may limit the usable brightness applied to the periphery by obscuring the image from the environment that we wish to preserve on the fovea. Furthermore, the peripheral retina serves an important function in alerting a person to moving objects, thereby warning of dangers, etc. This may limit the use to relatively quiet, safe environments. Also, the psychological effects of viewing the world through a restricted opening in a bright field may not be acceptable. The converse situation in which the surround is dark we expect will be very tolerable, perhaps even pleasant. We note that Eskimos have long used devices with horizontal slit-shaped apertures to shield most of the retina from snow glare. Apparently the wearer can function quite normally with this restructure of field of view. It is possible that the slit aperture may permit normal freedom of movement in the case of the bright periphery as well.

Additionally, the development of instrumentation to measure light exposure would facilitate the implementation of the preferred embodiments. For example, a light meter could be developed which would measure brightness as given by B=0.069I^(1/3) above. The ability of such a meter to integrate light exposure over an entire day would greatly facilitate the calculation of a phased stimulus vector and could allow individuals to more closely monitor their effective dose of light.

b. Devices for the Administration of Darkness

Use of some of the methods of the invention requires that individuals be shielded from light or exposed only to attenuated light. A person may be shielded from incident light by placing him or her in a dark windowless room or by placing an opaque material over his or her eyes.

As an alternative to constructing a windowless room, the windows of a normal room such as a hospital room, hotel room, or private bedroom can be modified by covering all windows with shutters or shades designed to totally exclude light. Many such devices are used for photographic darkrooms and are highly effective. One type uses an opaque screen that slides in a frame running completely around the window opening. Black velvet-like surfaces seal out light all the way around the frame when the screen is closed. The screen opens by sliding upward in the frame and rolling up at the top, which allows normal use of the window. For short-term use, a simple "blackout curtain" of flexible opaque material, covering the window and adhered around the edges is also effective.

Some circumstances require that a person be shielded from bright light while active and able to see. Devices for reducing the light coming into a person's eye, while still permitting vision, are needed. Goggles and masks that uniformly attenuate all incident light are commonly used as safety devices by welders and other workers whose work exposes them to hazardously bright light. These same devices may be applied to the methods here when light attenuation is needed. The device must block light from all directions with opaque material or a material of a low transmissivity of approximately one to ten percent.

Another device serving a similar function has long been used by Eskimos to protect from snow glare. It has the form of an opaque eye or face covering with a horizontal slit-shaped aperture. The aperture admits sufficient light and a sufficient view area to allow normal movement while surrounding most of the eye with a dark field.

Advantageously, the light admitted by a light attenuating device may vary according to ambient conditions, blocking the light more completely in bright light or daylight and admitting more light when the surroundings are dark. This characteristic makes such a device safer and more effective, and it can be achieved in a variety of ways. Photochemically sensitive coatings exist that darken when exposed to brighter light; they are commonly used in sunglasses. Such a coating, but with a generally greater saturation level, would be applicable, or existing coatings can be used in conjunction with a conventional light attenuating filter.

More precise control is afforded by the use of an electronic device built into the goggles that senses the ambient light level and compensates accordingly, by mechanically widening or narrowing the viewing aperture with a small motor, or by rotating one polarized filter element relative to another to change the transmissivity, or by activating a translucent material or coating that changes its transmissivity in response to a small voltage placed across it.

C. Devices for the Scheduling and Timing of Therapeutic Light and Darkness

The methods and formulae described for determining the ideal scheduling of periods of light and darkness to achieve a desired phase or amplitude change for a given individual can be put into effect in a variety of ways. A physician or other person trained in the method can make the determination for an individual; this is appropriate in cases where the change is to be effected for therapeutic reasons such as the treatment of affective personality disorders or the treatment of delayed sleep phase insomnia. However, other applications of the technique, such as treatment of jet lag or to facilitate adaptation to shift change transitions for workers, may benefit from devices that automate or simplify the calculation of light and darkness schedules based on the formulae of the mathematical model developed herein.

A computer program can be created for any given computer device that performs the relevant calculations. The program queries the user about his or her sleep characteristics and the nature of the change desired. The program allows the user to express this information in nontechnical language--for example, in the case of jet lag amelioration, it would ask the origin and destination locations and the times of the airline flights; the user would not need to know the longitudes of the locations or any of the principles behind the method. The program would inform the user what times to schedule light and darkness.

For general users such as frequent business travelers, the program can be made to run on personal or business computers, and can be sold and distributed in a variety of media including magnetic disks, magnetic tapes, optical disks, direct loading via modem, printed code strips, paper tapes, and source code listings on paper. For larger-scale users such as airlines, the program incorporating the method can itself be incorporated into existing multipurpose computer systems. In the case of airlines, such a subsystem can dispense recommended light and darkness schedules for jet lag reduction along with other flight information.

The method can also be incorporated into small dedicated devices such as "smart" wristwatches or calculators, ideal for frequent travelers or shift workers. A slide rule device, either linear or circular, can be created that allows the user to determine a schedule by setting parameters and reading results from sliding analog scales. A coin-operated electronic device that queries the user and dispenses the information for a fee can be placed in public places, particularly in airports.

Timing and scheduling mechanisms can also be built into the light fixtures and installations themselves. These devices would determine the proper times and automatically turn the lights on when appropriate. This is particularly effective where lights are installed in workplaces (for shift change adjustment) or in airport waiting areas and aircraft (for jet lag compensation) since they would operate on programmed schedules without human intervention.

d. Installations Incorporating the Devices

There are many ways that the methods and devices described herein can be implemented to provide a service to those that would benefit from them. Hospitals, factories, and utilities which operate around the clock can install overhead fixtures with sufficient lighting capacities to effect the method. Computers programmed with the operation's shift schedules could operate the lights routinely and automatically for the benefit of workers.

Hospitals and medical facilities providing care to persons with affective disorders or sleep scheduling disorders can equip certain rooms with opaque window screens and banks of wall or ceiling mounted lights to allow the patient to be exposed to light and/or darkness as required for their treatment. These rooms can also be equipped with the necessary apparatus for carrying out the phase-assessment diagnostic procedure before and/or after therapy. Patients can use home appliances for exposure to lights at specific times of day as ordered by a physician. Light and/or darkness goggles can also be used to augment this treatment. Hotels catering to international air travelers can install bright lights in bedrooms or in a central facility, and darkness curtains in bedrooms, thus creating a special service to customers likely to suffer from jet lag. A computer, coin operated or operated by hotel desk personnel, will dispense information to individual guests on the best times of exposure. A dedicated `salon` operating independently from hotels could also provide this service in the same way that ultraviolet tanning salons operate today. Airports and airlines can install equipment allowing them to offer a special class of service providing facilities for passengers to be exposed to amplified or reduced lighting to aid in their adaptation to new time zones. This equipment can include bright lights installed in special airport lounges or in the aircraft themselves.

Frequent travelers may be willing to purchase personal portable equipment such as light/darkness goggles and exposure time calculators to facilitate their own adjustment to shifting time zones. Military and aerospace facilities and vehicles can utilize equipment similar to that described for civilian airports and aircraft, in order to help critical personnel adapt to shifting operational schedules or transmeridian travel without loss of performance.

Spacecraft, submarines, machine rooms, isolated research environments, hospital intensive care areas, and all other environments where people must live and work while isolated from the external environment can utilize schedules of bright and subdued light, designed in accordance with the methods herein, to improve the health and the sleep hygiene of their occupants.

As stated above, there are several potential uses of this invention, namely to help shift workers adapt to variable work schedules, reduce jet lag, and treat patients with a variety of medical disorders. Specifically, factories, hospitals and utilities which operate around the clock could install overhead fixtures with sufficient lighting capacity to employ this new process to facilitate adaptation of the workers to their persistently changing work schedules. In wintertime, the indoor lights could be used to provide heat for the facilities.

In addition, the process could be used by several components of the travel industry. With development of proper hardware, international air carriers could initiate a special class of service providing facilities for passengers to be exposed to amplified or reduced lighting at times designed to aid in their adaptation to their destination time zone. Airport and other hotels catering to the international business traveler could have sunlight simulator suites where guests could be exposed to lights prior to or after a trip. Finally, with appropriate miniaturization, it may be possible for consumers to purchase "sunglasses" which would actually emit light such that the retina would be exposed to the intensity of light required to achieve the desired effect.

Patients with medical disorders could use home appliances for exposure to the lights at a specific time of day. This could be conducted in conjunction with a diagnostic procedure before and/or after the administration of the phototherapy. Patients likely to benefit would include those with delayed, advanced, or hypernycthemeral sleep syndromes, and potentially patients with psychiatric disorders.

8. Conclusion

Whereas various particular embodiments of the present invention have been disclosed in detail above, it is to be understood that they are presented by way of example, and not limitation. Thus, the full scope and import of the present invention should not be limited by any of the embodiments described above, but should be defined only in accordance with the following claims. 

What is claimed is:
 1. A method of modifying a human subject's endogenous circadian cycle to a desired state, comprising the steps of:determining the characteristics of a desired endogenous circadian cycle for said subject; selecting an appropriate time with respect to the presumed phase of physiological markers of the present endogenous circadian cycle for said subject during which to apply a light stimulus to effect a desired modification of said present endogenous circadian cycle of said subject; and applying said light stimulus at said selected appropriate time to achieve said desired endogenous circadian cycle for said subject.
 2. The method of claim 1 wherein said light stimulus is enhanced illumination.
 3. The method of claim 1 wherein said light stimulus includes diminished illumination.
 4. The method of claim 1 wherein said light stimulus includes ambient light.
 5. The method of claim 1 wherein said stimulus includes a combination of enhanced illumination and diminished illumination.
 6. The method of claim 1 further comprising the step of:assessing the characteristics of the present endogenous circadian cycle of said subject, and wherein said appropriate time is selected based on said desired characteristics.
 7. The method of claim 1 wherein said light stimulus includes light of an intensity greater than 2000 lux.
 8. The method of claim 7 wherein said light intensity is inferred at a position approximately at the pupil of said subject.
 9. The method of claim 1 wherein said light stimulus includes light of an intensity between zero and 100,000 lux.
 10. The method of claim 9 wherein said intensity is inferred at a position approximately at the pupil of said subject.
 11. A method of facilitating the physiological adaptation of a human subject to a reoccurring activity/rest-leisure schedule requiring said subject to be active during a portion of conventional sleep hours, comprising the steps of:selecting a substantial episode of time during the activity portion of said subject's activity/rest schedule to apply a light stimulus; and applying, at said selected time episode, said light stimulus consisting of an episode of enhanced illumination; whereby the physiological adaptation of said subject to a reoccurring activity/rest schedule requiring said subject to be active during a portion of said conventional sleep hours if facilitated.
 12. The method of claim 11 wherein the selection of said time is based on a determination of the characteristics of a desired sleep time for said subject.
 13. The method of claim 11 wherein the selection of said time is based on a determination of the characteristics of a desired wake time for said subject.
 14. The method of claim 11 wherein said selected time occurs between the hours of 11:30 p.m. and 7:30 a.m.
 15. The method of claim 11 wherein said selected time occurs during the entire activity portion of said subject's schedule.
 16. The method of claim 11 further comprising the step of:exposing said subject to an ambient level of illumination during a second selected time of the activity portion of said subject's schedule.
 17. The method of claim 11 further comprising the step of:providing said subject with appropriate equipment to enable said subject to diminish the level of illumination to which they are exposed during the rest-leisure portion of said subject's schedule.
 18. The method of claim 11 wherein said enhanced illumination is light having an intensity greater than 2000 lux.
 19. The method of claim 18 wherein said intensity is inferred at a position approximately at the pupil of the subject.
 20. A method of facilitating the physiological adaptation of a human subject to an activity/rest schedule requiring said subject to be active during a portion of the conventional sleep hours by modifying said subject's present endogenous circadian cycle to a desired state, comprising the steps of:determining the characteristics of a desired endogenous circadian cycle for said subject; selecting an appropriate time episode with respect to the presumed phase of physiological markers of the present endogenous circadian cycle for said subject during which to apply a light stimulus to effect a desired modification of said present endogenous circadian cycle; and exposing said subject to said light stimulus at said selected time episode; whereby the endogenous circadian cycle of said subject is modified to a desired state, thereby facilitating the physiological adaptation of said subject to an activity/rest schedule requiring said subject to be active during a portion of said conventional sleep hours.
 21. The method of claim 20 wherein said selected time occurs between the hours of 11:30 p.m. and 7:30 a.m.
 22. The method of claim 20 wherein said selected time occurs during the entire activity portion of said subject's schedule.
 23. The method of claim 20 further comprising the step of:exposing said subject to a diminished level of illumination during a second selected time of the rest portion of said subject's schedule.
 24. The method of claim 20 wherein said light stimulus includes light of an intensity greater then 2000 lux.
 25. The method of claim 24 wherein said intensity is inferred at a position approximately at the pupil of said subject.
 26. The method of claim 20 wherein said light stimulus includes light of an intensity between zero and 100,000 lux.
 27. The method of claim 26 wherein said intensity is inferred at a position approximately at the pupil of said subject.
 28. A method of improving the physiological adaptation of the endogenous circadian pacemaker of a human subject to a desired wake time by resetting the phase of said endogenous circadian pacemaker, said method comprising the steps of:estimating the phase of the endogenous circadian cycle of said subject based on characteristics of said subject's habitual sleep/wake cycle; selecting an appropriate time during said estimated phase of said circadian cycle of said subject based on the presumed phase of physiological markers of the circadian cycle of said subject during which to expose said subject to a stimulus including an enhanced level of illumination; and exposing said subject to said stimulus at said selected time to thereby reset the phase of said endogenous circadian pacemaker of said subject.
 29. The method of claim 28 wherein said subject is exposed to said stimulus at a time preceding said subject's desired bedtime to thereby delay the endogenous circadian pacemaker of said subject.
 30. The method of claim 28 wherein said subject is exposed to said stimulus at a time following said subject's desired wake time to thereby advance the endogenous circadian pacemaker of said subject.
 31. The method of claim 30 wherein said subject is awake during exposure to said stimulus.
 32. The method of claim 28 wherein said stimulus includes light of an intensity greater than 2000 lux.
 33. The method of claim 32 wherein said intensity is inferred at a position approximately at the pupil of said subject.
 34. A method of improving the physiological adaptation of the endogenous circadian pacemaker of a human subject to a desired wake time by resetting the phase of said endogenous circadian pacemaker, said method comprising the steps of:determining the characteristics of a desired endogenous circadian cycle for said subject; selecting an appropriate time with respect to the presumed phase of physiological markers of the present endogenous circadian cycle for said subject during which to expose said subject to a stimulus including an enhanced level of illumination; and exposing said subject to said stimulus at said selected time to thereby reset the phase of said endogenous circadian pacemaker of said subject.
 35. The method of claim 34 wherein said subject is exposed to said stimulus at a time preceding said subject's desired bedtime to thereby delay the endogenous circadian pacemaker of said subject.
 36. The method of claim 34 wherein said subject is exposed to said stimulus at a time following said subject's desired wake time to thereby advance the endogenous circadian pacemaker of said subject.
 37. The method of claim 36 wherein said subject is awake during exposure to said stimulus.
 38. The method of claim 34 wherein said stimulus includes light of an intensity greater than 2000 lux.
 39. The method of claim 38 wherein said intensity is inferred at a position approximately at the pupil of said subject. 